Iodoshield Active

Dosage Form: FOR ANIMAL USE ONLY
IODOSHIELD
ACTIVE

Iodine based teat sanitizer with Manuka honey from New Zealand
Spray or Dip concentrate
For Commercial Use Only

An aid in reducing the spread of organisms which may cause bovine mastitis.
The product contains the active ingredient at 0.19 pounds per gallon.

USE RATES

FOR ROUTINE SPRAY OR DIP APPLICATIONS
Dilute 1 part FIL Iodoshield Active with 9 parts water.

IN EARLY LACTATION OR INCLEMENT WEATHER CONDITIONS
Dilute 1 part FIL Iodoshield Active with 4 parts water.

GENERAL INSTRUCTIONS

Make up use solutions in clean plastic or stainless steel containers using potable water. Use solutions are reasonably stable if stored in a clean and contamination free environment. However, it is recommended that only sufficient product for a week's use should be made up at one time.

Apply to teats as soon as possible after cup removal. Ensure that the whole teat surface is covered. This product contains a high level of emolliency and generally should not need additional emollient. PRECAUTION: As with any germicide, irritation may occur in sensitive animals. If irritation occurs, discontinue use and consult your veterinarian.

PRECAUTIONARY STATEMENTS HAZARDS TO HUMANS (AND DOMESTIC ANIMALS)

Prolonged or frequently repeated skin contact may cause allergic reaction in some individuals. Remove contaminated clothing and wash before reuse.

CAUTION

Causes moderate eye irritation. Avoid contact with eyes, skin or clothing. Wear protective eyewear (Goggles, face shield or safety glasses). Harmful if swallowed or absorbed through skin or inhaled. Avoid breathing spray mist. Wash thoroughly with soap and water after handling and before eating, drinking, chewing gum, using tobacco or using the toilet. Remove and wash contaminated clothing before reuse. Wear rubber gloves when handling or applying.

FIRST AID

IF IN EYES: Hold eye open and rinse slowly and gently with water for 15-20 minutes. Remove contact lenses, if present, after the first 5 minutes, then continue rinsing. Call a poison control center or doctor for treatment advice.

IF SWALLOWED: Call a poison control center or doctor immediately for treatment advice. Have person sip a glass of water if able to swallow. Do not induce vomiting unless told to by a poison center or doctor.

IF ON SKIN: Take off contaminated clothing. Rinse skin immediately with plenty of water for 15-20 minutes. Call a poison control center or doctor for treatment.

IF INHALED: Move person to fresh air. If person is not breathing, call 911 or an ambulance, then give artificial respiration, preferably mouth-to-mouth, if possible. Call a poison control center or doctor for further treatment.

Have the product container or label with you when calling a poison control center or doctor, or going for treatment. You may also contact 1-800-328-0026 for emergency medical treatment information.

ENVIRONMENTAL HAZARDS

Do not discharge effluent containing this product into lakes, streams, ponds, estuaries, oceans, or other waters unless in accordance with the requirements of a National Pollutant Discharge Elimination System (NDPES) permit and the permitting authority has been notified in writing prior to discharge. Do not discharge effluent containing this product to sewer systems without previously notifying the local sewage treatment plant authority.

For guidance contact your State Water Board or Regional Office of the EPA. Do not contaminate water by cleaning of equipment or disposal of waste.

STORAGE AND DISPOSAL

Do not contaminate water, food or feed by storage or disposal. Open dumping is prohibited. Do not reuse empty container. Protect from freezing.

PRODUCT STORAGE: Store the product in a dry and cool place, where it is not reachable by children.

PRODUCT DISPOSAL: Wastes resulting from use of this product may be disposed of on site or at an approved waste disposal facility.

CONTAINER DISPOSAL: Do not reuse containers. Triple rinse containers when empty. Add rinses to use solutions.

GENERAL: Consult federal, state, or local disposal authorities for approved alternative procedures such as limited open burning.

Manufactured by: Farmers Industries (New Zealand) Limited, 72 Portside Drive, PO Box 4144 Mt Maunganui, New Zealand.

TEL +64 7 575 2162 WWW.FIL.CO.NZ

Distributed by FIL Agritech, LLC 5983 US Rte 11 Homer, NY 13077

TOLL FREE 1-800-680-3167 WWW.FILAGRITECH.COM

PRINCIPAL DISPLAY PANEL - 20 L Bottle Label

CAUTION
KEEP OUT OF REACH OF CHILDREN

FIL

FARM INNOVATION / ANIMAL HEALTH

IODOSHIELD
ACTIVE

Contains 2.2% Iodine and 97.8% other ingredients

Iodine based teat sanitizer with
Manuka honey from New Zealand
Spray or Dip concentrate
For Commercial Use Only

An aid in reducing the spread of organisms
which may cause bovine mastitis

WWW.FIL.CO.NZ

Iodoshield Active 
iodine  concentrate Product Information Product Type OTC ANIMAL DRUG NDC Product Code (Source) 51546-001 Route of Administration TOPICAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength iodine (iodine) iodine 86.2 g  in 4.55 L Inactive Ingredients Ingredient Name Strength sorbitol   honey   water   lanolin   alcohol   Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 51546-001-02 20 L In 1 BOTTLE None 2 51546-001-20 200 L In 1 DRUM None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED DRUG OTHER 06/01/2010
Labeler - Farmers Industries (New Zealand) Limited (590180329) Establishment Name Address ID/FEI Operations Farmers Industries (New Zealand) Limited 590180329 MANUFACTURE Revised: 08/2010Farmers Industries (New Zealand) Limited

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Lipobase

1. Name Of The Medicinal Product

Lipobase.

2. Qualitative And Quantitative Composition

Lipobase contains no active ingredient.

3. Pharmaceutical Form

Cream.

4. Clinical Particulars 4.1 Therapeutic Indications

For use where it is desired by the physician to reduce gradually the topical dosage of Locoid Lipocream. It may also be used where a continuously alternating application of the active product and the base is required e.g. in prophylactic therapy. Application of the Lipobase is also recommended where it is felt by the physician that the use of a bland emollient base is preferable to the cessation of therapy with the active product. Lipobase may also be used as a diluent for the active product in those cases where dilution is regarded as necessary by the prescriber. Lipobase may also be used other than in conjunction with a topical corticosteroid for its emollient action, and for the treatment of mild skin lesions such as pruritus or dry, scaly skin, where topical corticosteroid is not warranted.

4.2 Posology And Method Of Administration

For adults, children and the elderly: Lipobase may be used either by replacing an application of the active product or alternating the application of the active product and the base, gradually diminishing the application of the active product until therapy ceases, or by the application of the product for its emollient action.

4.3 Contraindications

None stated.

4.4 Special Warnings And Precautions For Use

A small number of people may be hypersensitive (allergic) to the constituents of Lipobase.

Cetostearyl alcohol may cause local skin reactions (e.g. contact dermatitis).

Methyl parahydroxybenzoate may cause allergic skin reactions (possibly delayed).

4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction

None stated.

4.6 Pregnancy And Lactation

None stated.

4.7 Effects On Ability To Drive And Use Machines

None stated.

4.8 Undesirable Effects

None stated.

4.9 Overdose

None stated.

5. Pharmacological Properties 5.1 Pharmacodynamic Properties

The product acts topically as an emollient cream.

5.2 Pharmacokinetic Properties

Topical administration with no pharmacologically active constituents.

5.3 Preclinical Safety Data

No relevant preclinical safety data has been generated.

6. Pharmaceutical Particulars 6.1 List Of Excipients

Cetostearyl alcohol

Macrogol cetostearyl ether

Light liquid paraffin

White soft paraffin

Methyl parahydroxybenzoate

Sodium citrate, anhydrous

Citric acid, anhydrous

Purified water

6.2 Incompatibilities

None stated.

6.3 Shelf Life

30g, 50g, 100g and 200g packs, 3 years.

200g and 500g packs, 2 years

6.4 Special Precautions For Storage

Do not store above 25°C.

6.5 Nature And Contents Of Container

Collapsible aluminium tube with plastic screw cap containing 30 g, 50 g, 100 g or 200 g; and pump dispenser containing 200 g or 500 g.

6.6 Special Precautions For Disposal And Other Handling

Not applicable.

7. Marketing Authorisation Holder

Astellas Pharma Ltd

Lovett House

Lovett Road

Staines

TW18 3AZ

United Kingdom

8. Marketing Authorisation Number(S)

PL0166/0125

9. Date Of First Authorisation/Renewal Of The Authorisation

First authorisation granted 19 February 1985

Renewal granted 23 January 2001.

10. Date Of Revision Of The Text

7th February 2007

11. Legal category

P

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Sodium Fluoride Chewable Tablets

Fluoride Chewable Tablets 1 mg

Active Ingredient: 1 mg of fluoride ion from 2.2 mg of sodium fluoride (NaF).

Inactive Ingredients: Lactose, Saccharine, Cherry Flavor, D&C Red #7 Calcium Lake, Magnesium Stearate.

DOSAGE AND ADMINISTRATION:

Dissolve in the mouth or chew before swallowing, preferably at bedtime after brushing teeth.

STORAGE:

Store at a Controlled Room Temperature 20?-25?C (68?-77?F)

743634

Manufactured for:
Libertas Pharma, Inc.
Lawrenceville, GA 30043
Iss. 03/11   172-12

Container Label

NDC 51862-172-12

Fluoride Chewable Tablets

1 mg

(From 2.2 mg of Sodium Fluoride)

Cherry Flavor       120 Tablets       Rx Only

Libertas
Pharma Inc.

FLUORIDE 
fluoride  tablet, chewable Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 51862-172 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM FLUORIDE (FLUORIDE ION) FLUORIDE ION 1 mg Inactive Ingredients Ingredient Name Strength CHERRY   LACTOSE   SACCHARIN   D&C RED NO. 7   MAGNESIUM STEARATE   Product Characteristics Color RED Score no score Shape ROUND Size 6mm Flavor CHERRY Imprint Code 172 Contains          Packaging # NDC Package Description Multilevel Packaging 1 51862-172-12 120 TABLET In 1 BOTTLE None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved drug other 05/21/2011
Labeler - Libertas Pharma, Inc. (962128943) Revised: 05/2011Libertas Pharma, Inc.

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Vet One Chlorhexidine

Dosage Form: FOR ANIMAL USE ONLY
MWI/Vet One 2% Chlorhexidine solution MWI/Vet One 2% Chlorhexidine solution

ACTIVE INGREDIENTS:
2% Chlorhexidine Gluconate.

CAUTION:
Avoid contact with eyes and mucous membranes. This product is not to be used in ears. If contact is made, flush immediately and thoroughly with clean water. For use on horses and dogs.

Product No. 1CHL008
8CHL008-108
Distributed by:
MWI
Meridian, ID 83680
(888) 694-8381
MWI/Vet One 2% Chlorhexidine solution

PRODUCT DESCRIPION:
A topical aqueous cleaning solution for use on horses and dogs for application to superficial cuts, abrasions or insect stings.

DILUTE:
1 ounce (2 tablespoons) of Chlorhexidine Solution per gallon of clean water.
DIRECTIONS FOR USE:
Rinse skin area to be treated with Chlorhexidine Solution. Wipe away excess and pat dry with sterilized gauze or sponge.
MWI/Vet One 2% Chlorhexidine solution

Vet One Chlorhexidine 
chlorhexidine gluconate  solution Product Information Product Type OTC ANIMAL DRUG NDC Product Code (Source) 13985-017 Route of Administration TOPICAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Chlorhexidine Gluconate (CHLORHEXIDINE) Chlorhexidine Gluconate 2 g  in 0.1 L Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 13985-017-80 3.785 L In 1 JUG None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/01/2010
Labeler - MWI VETERINARY SUPPLY CO (019926120) Revised: 01/2010MWI VETERINARY SUPPLY CO

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Evitex

Dosage Form: FOR ANIMAL USE ONLY
Evitex

Vitex agnus-castus
Liquid Chaste Berry

Active Ingredients:

Chasteberries [Vitex agnus-castus] 15mg per ml

Inactive Ingredients:

Acetic acid glacial and Propionic acid [organic preservatives[Salt,Water

FOR USE ON ANIMALS ONLY

Evitex contains NO animal parts or residues

Imported to the USA by :
Emerald Valley Natural Health Inc, Exeter, NH 03833
Batch No : 94429
Use by Date : 03/12/11
Evitex is manufactured in the UK by
SCA Nutec [Provimi Ltd]
Nutec Mill, Eastern Avenue
Lichfield, Staffordshire, WS13 7SE, UK
Exported by :
Equiglobal Ltd
Manningtree, Essex, CO11 1UT, UK
20 Litres/5.283 gallons [US]

Evitex 
chaste tree  extract Product Information Product Type PRESCRIPTION ANIMAL DRUG NDC Product Code (Source) 52338-388 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHASTE TREE (CHASTE TREE) CHASTE TREE 15 mg  in 1 mL Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 52338-388-20 20000 mL In 1 BOTTLE None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/01/2010
Labeler - SCA NuTec (233072193) Establishment Name Address ID/FEI Operations SCA NuTec 233072193 manufacture Revised: 04/2010SCA NuTec

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Immuzim

Dosage Form: FOR ANIMAL USE ONLY
Immuzim

Echinacea Sp.

Active Ingredients:

Echinacea [Echinacea angustifolia] 7.5mg per ml
Echinacea [Echinacea pallida] 7.5mg per ml

Inactive Ingredients:

Acetic acid glacial and Propionic acid [organic preservatives[Salt,Water

FOR USE ON ANIMALS ONLY

Immuzim contains NO animal parts or residues

Imported to the USA by :
Emerald Valley Natural Health Inc, Exeter, NH 03833
Batch No: 94414
Use by Date: 03/12/11
Immuzim is manufactured in the UK by
SCA Nutec [Provimi Ltd]
Nutec Mill, Eastern Avenue
Lichfield, Staffordshire, WS13 7SE, UK
Exported by :
Equiglobal Ltd
Manningtree, Essex, CO11 1UT, UK
20 Litres/5.283 gallons [US]

Immuzim 
echinacea angustifolia root and echinacea pallida root  extract Product Information Product Type PRESCRIPTION ANIMAL DRUG NDC Product Code (Source) 52338-398 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ECHINACEA ANGUSTIFOLIA ROOT (ECHINACEA ANGUSTIFOLIA ROOT) ECHINACEA ANGUSTIFOLIA ROOT 7.5   in 1 mL ECHINACEA PALLIDA ROOT (ECHINACEA PALLIDA ROOT) ECHINACEA PALLIDA ROOT 7.5   in 1 mL Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 52338-398-20 20000 mL In 1 BOTTLE None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/01/2010
Labeler - SCA NuTec (233072193) Establishment Name Address ID/FEI Operations SCA NuTec 233072193 manufacture Revised: 04/2010SCA NuTec

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Isopropyl Alcohol

MWI 99% Isopropyl Alcohol quart MWI 99% Isopropyl Alcohol quart

CONTAINS:

Active Ingredients:

   Isopropyl Alcohol .........................99%

Inert Ingredients:

   Water ...............................................1%

INDICATIONS: Widely used by veterinarians and artificial inseminators as a bactericide and antiseptic.
May also be used for temporary relief of minor muscular aches or pains caused by overexerction or fatigue. For use in manufacturing, processing or repacking. 

DIRECTIONS FOR USE: Dilute with water as desired. Scrub hands and arms with soap and water. Rinse with water and then scrub with alcohol. As a rub-down, apply full-strength directly to the affected area. Wet thoroughly and massage briskly to stimulate circulation.

MWI 99% Isopropyl Alcohol quart

WARNING: Flammable Liquid

For External Use Only

STORAGE: Store at controlled room temperature between 10 and 30 C(50 - 85F). Keep away from heat and open flame. Keep container closed when not in use.

MADE IN USA         TAKE TIME          OBSERVE LABEL DIRECTIONS

Distributed by:
MWI
Meridian, ID 83680
(888) 694-8381
www.vetone.net

MWI 99% Isopropyl Alcohol quart jug213332 innercase213332 outercase213332

Isopropyl Alcohol 
Isopropyl Alcohol  liquid Product Information Product Type OTC ANIMAL DRUG NDC Product Code (Source) 13985-330 Route of Administration TOPICAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Isopropyl Alcohol (Isopropyl Alcohol) Isopropyl Alcohol 99 L  in 100 L Inactive Ingredients Ingredient Name Strength WATER 1 L  in 100 L Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 13985-330-91 4 BOX In 1 CASE contains a BOX (13985-330-90) 1 13985-330-90 4 JUG In 1 BOX This package is contained within the CASE (13985-330-91) and contains a JUG (13985-330-89) 1 13985-330-89 0.946 L In 1 JUG This package is contained within a BOX (13985-330-90) and a CASE (13985-330-91)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/01/2010
Labeler - MWI/Vet One (019926120) Revised: 05/2010MWI/Vet One

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Rifamycin derivatives

A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

Rifamycin derivatives are antibiotics that work by binding to and inhibiting the mycobacterial DNA dependent RNA polymerase. These antibiotics are bacteriocidal and therefore extremely effective antituberculosis agents, but resistance can develop rapidly if used as a single agent. They easily penetrate into cells, body fluids and cerebrospinal fluid so can be used against organisms in the extracellular component and those that may be present in cells such as macrophages. Rifamycin antibiotics should be used throughout the course of tuberculosis treatment, which can be between nine months to a year.

See also

Medical conditions associated with rifamycin derivatives:

Bartonellosis Endocarditis Haemophilus influenzae Prophylaxis Legionella Pneumonia Leprosy Leprosy, Borderline Leprosy, Tuberculoid Meningitis Meningococcal Meningitis Prophylaxis Mycobacterium avium-intracellulare, Prophylaxis Mycobacterium avium-intracellulare, Treatment Nasal Carriage of Staphylococcus aureus Tuberculosis, Active Tuberculosis, HIV Positive Tuberculosis, Latent Tuberculosis, Prophylaxis Drug List: Rifadin Mycobutin Priftin Rifadin-Iv Rimactane

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Other immunosuppressants

A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

See also

Medical conditions associated with other immunosuppressants:

Acute Lymphoblastic LeukemiaAcute Lymphocytic LeukemiaAcute Nonlymphocytic LeukemiaAnemiaAsthma, MaintenanceAtopic DermatitisAutoimmune HepatitisBehcet's DiseaseBiliary CirrhosisBladder CancerBrain TumorBreast CancerBullous PemphigoidCervical CancerChoriocarcinomaChronic Active HepatitisChronic Inflammatory Demyelinating PolyradiculoneuropathyCogan's SyndromeColorectal CancerCrohn's DiseaseCrohn's Disease, AcuteCrohn's Disease, MaintenanceDermatomyositisEctopic PregnancyEczemaEsophageal CarcinomaGastric CancerGlomerulonephritisGraft-versus-host diseaseHead and Neck CancerHodgkin's LymphomaIdiopathic Thrombocytopenic PurpuraInflammatory Bowel DiseaseLeprosy, Erythema Nodosum LeprosumLymphomaMeningeal LeukemiaMultiple MyelomaMultiple SclerosisMyasthenia GravisMycosis FungoidesMyopathyNeoplastic DiseasesNephrotic SyndromeNeurosarcoidosisNon-Hodgkin's LymphomaNon-Small Cell Lung CancerOrgan Transplant, Rejection ProphylaxisOsteosarcomaOvarian CancerPancreatic CancerPemphigoidPemphigusPityriasis rubra pilarisPsoriasisPsoriatic ArthritisRenal TransplantRheumatoid ArthritisSarcoidosisSmall Cell Lung CancerSoft Tissue SarcomaSolid TumorsSystemic Lupus ErythematosusSystemic SclerosisTakayasu's ArteritisTrophoblastic DiseaseUlcerative ColitisUveitis Drug List:RevlimidXolairAzasanImuranRheumatrexThalomidTrexall

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Teat Dip 5000

Dosage Form: FOR ANIMAL USE ONLY

FOR COMMERCIAL USE ONLY

KEEP OUT OF REACH OF CHILDREN

NOT FOR HUMAN USE

CAUTION

CAUTION

Harmful if swallowed, eye irritant.

FIRST AID:

Avoid contact with skin and eyes. Contact can cause severe irritation. Get medical attention. If ingested, drink large amounts of water or milk. DO NOT induce vomiting.

Get immediate attention. Avoid repeated contact with skin and hands. Use rubber gloves to avoid skin irritation. If contact occurs, wash thoroughly with clean water.

EMERGENCY: CHEMTREC 800-424-9300

Prior to milking, dip teats in undiluted Teat Dip 5000. Wipe off with a clean towel after 15 to 30 seconds.

After milking apply Teat Dip 5000 by dipping. Do not rinse or wash off. Allow teats to dry before letting cows

outdoors in cold weather to guard against chapping.

Teat Dip 5000
Iodine Teat Dip
An aid in Reducing the Spread of Organisms
Which May Cause Mastitis
ACTIVE INGREDIENTS:
Iodine..................................................0.5%
INACTIVE INGREDIENTS....................99.5%
Teat Dip 5000 
iodine  solution Product Information Product Type OTC ANIMAL DRUG NDC Product Code (Source) 64892-002 Route of Administration TOPICAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IODINE (IODINE) IODINE 0.5 L  in 100 L Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 64892-002-16 18.9 L In 1 DRUM None 2 64892-002-17 56.78 L In 1 DRUM None 3 64892-002-18 113.6 L In 1 DRUM None 4 64892-002-21 208.2 L In 1 DRUM None 5 64892-002-88 1040 L In 1 DRUM None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/14/2000
Labeler - Wausau Chemical (006136220) Establishment Name Address ID/FEI Operations Wausau Chemical 006136220 manufacture Revised: 09/2000Wausau Chemical

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Udder Wash Concentrate175

Dosage Form: FOR ANIMAL USE ONLY

FOR COMMERCIAL USE ONLY

KEEP OUT OF REACH OF CHILDREN

NOT FOR HUMAN USE

CAUTION

CAUTION

Harmful if swallowed, eye irritant.

FIRST:

Avoid contact with skin and eyes. Contact can cause severe irritation. Get medical attention. If ingested, drink

large amounts of water or milk. DO NOT induce vomiting. Get immediate attention. Avoid repeated contact with

skin and hands. Use rubber gloves to avoid skin irritation. If contact occurs, wash thoroughly with clean water.

EMERGENCY: CHEMTREC 800-424-9300

UDDER WASH #175 is a concentrated product containing a minimum of 1.75% titratable iodine.

UDDER WASH #175 diluted at one once per five gallons of water produces an efficient washing

solution of minimum of 25 parts per million (ppm).

Utter Wash Concntrate #175
Iodine Utter Wash
An aid in Reducing the Spread of Organisms
Which May Causes Mastitis
ACTIVE INGREDIENTS:
Iodine...........................................1.75%
INACTIVE INGREDIENTS..............98.25%
Wausau Chemical Corporation
2001 North River Drive
Wausau, WI 54403-0953 U.S.A.
UDDER WASH CONCENTRATE 175 
iodine  solution Product Information Product Type OTC ANIMAL DRUG NDC Product Code (Source) 64892-005 Route of Administration TOPICAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IODINE (IODINE) IODINE 1.75 L  in 100 L Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 64892-005-16 18.9 L In 1 DRUM None 2 64892-005-17 56.78 L In 1 DRUM None 3 64892-005-18 113.6 L In 1 DRUM None 4 64892-005-21 208.2 L In 1 DRUM None 5 64892-005-88 1040 L In 1 CONTAINER None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/14/2000
Labeler - Wausau Chemical (006136220) Establishment Name Address ID/FEI Operations Wausau Chemical 006136220 manufacture Revised: 09/2000Wausau Chemical

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Kids Choice

Dosage Form: gel, dentifrice
ACTIVE INGREDIENT

Active Ingredient: Stannous Fluoride

INACTIVE INGREDIENTS

Glycerine, Hydroxy Ethyl Celluulose, Xylitol

USE

Aids in the prevention of dental decay.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

DIRECTIONS FOR USE

Adults and Children 12 years and Older: Use after regular brushing and flossing.  Place gel across length of toothbrush.  Brush Thoroughly.  Keep on teeth for 1 - 1 1/2 minutes and then expectorate (spit out).  Do not swallow.  Use once a day for cavity prevention.  Supervise children until capable of using without supervision.
Children 6-11 Years:  See directions above.  Adult supervision required.
Children Under 6: Consult a Dentist or Physician.

OTHER INFORMATION

This is a fluoride prevention treatment gel, not a toothpaste.  Read directions carefully before use.  This product may produce surface discoloration of the teeth.  Adequate toothbrushing may prevent discoloration.  Discoloration is not harmful or permanent and may be removed by a dental professional.  Do not freeze or expose to extreme heat.

QUESTIONS ? COMMENTS ?

Questions?? Comments??
Call 1-479-787-5168 M-F 9am to 5pm CST

Warnings

If more than amount used for brushing is accidentally swallowed, seek medical help from a poison control center.

PACKAGE LABEL

Brush on Therapy for Cavity Prevention - Doctor's Choice 0.4% Stannous Fluoride Gel
Manufactured by Massco Dental

Kids Choice 
stannous fluoride  gel, dentifrice Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 63783-005 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength STANNOUS FLUORIDE (FLUORIDE ION) STANNOUS FLUORIDE .45103 g  in 120 g Inactive Ingredients Ingredient Name Strength GLYCERIN   HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)   XYLITOL   Product Characteristics Color      Score      Shape Size Flavor BUBBLE GUM (BUBBLE GUM) Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 63783-005-04 120 g In 1 BOTTLE, DISPENSING None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part355 01/01/1989
Kids Choice 
stannous fluoride  gel, dentifrice Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 63783-006 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength STANNOUS FLUORIDE (FLUORIDE ION) STANNOUS FLUORIDE .4510 g  in 120 g Inactive Ingredients Ingredient Name Strength GLYCERIN   HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)   XYLITOL   Product Characteristics Color      Score      Shape Size Flavor CREME DE MENTHE (HINT OF MINT) Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 63783-006-04 120 g In 1 BOTTLE, DISPENSING None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part355 01/01/1989
Kids Choice 
stannous fluoride  gel, dentifrice Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 63783-007 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength STANNOUS FLUORIDE (FLUORIDE ION) STANNOUS FLUORIDE .4510 g  in 120 g Inactive Ingredients Ingredient Name Strength GLYCERIN   HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)   XYLITOL   Product Characteristics Color      Score      Shape Size Flavor LIME (LIMEAIDE) Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 63783-007-04 120 g In 1 BOTTLE, DISPENSING None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part355 01/01/1989
Kids Choice 
stannous fluoride  gel, dentifrice Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 63783-008 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength STANNOUS FLUORIDE (FLUORIDE ION) STANNOUS FLUORIDE .4510 g  in 120 g Inactive Ingredients Ingredient Name Strength GLYCERIN   HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)   XYLITOL   Product Characteristics Color      Score      Shape Size Flavor GRAPE (GRAPE) Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 63783-008-04 120 g In 1 BOTTLE, DISPENSING None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part355 01/01/1989
Kids Choice 
stannous fluoride  gel, dentifrice Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 63783-009 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength STANNOUS FLUORIDE (FLUORIDE ION) STANNOUS FLUORIDE .4510 g  in 120 g Inactive Ingredients Ingredient Name Strength GLYCERIN   HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)   XYLITOL   Product Characteristics Color      Score      Shape Size Flavor CHERRY (CHERRY) Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 63783-009-04 120 g In 1 BOTTLE, DISPENSING None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part355 01/01/1989
Kids Choice 
stannous fluoride  gel, dentifrice Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 63783-015 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength STANNOUS FLUORIDE (FLUORIDE ION) STANNOUS FLUORIDE .4510 g  in 120 g Inactive Ingredients Ingredient Name Strength GLYCERIN   HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)   XYLITOL   Product Characteristics Color      Score      Shape Size Flavor COTTON CANDY (COTTON CANDY) Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 63783-015-04 120 g In 1 BOTTLE, DISPENSING None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part355 01/01/1989
Labeler - Massco Dental A Division of Dunacin Pharmaceuticals (008081858) Registrant - Massco Dental A Division of Dunacin Pharmaceuticals (008081858) Establishment Name Address ID/FEI Operations Massco Dental A Division of Dunacin Pharmaceuticals 008081858 manufacture Revised: 10/2011Massco Dental A Division of Dunacin Pharmaceuticals
More Kids Choice resources Kids Choice Use in Pregnancy & Breastfeeding Kids Choice Support Group 3 Reviews for Kids Choice - Add your own review/rating Compare Kids Choice with other medications Prevention of Dental Caries

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Hex-Plus

Generic Name: chlorhexidine gluconate liquid
Dosage Form: FOR ANIMAL USE ONLY
Hex-Plus

USE DIRECTIONS:
Use at full strength, do not dilute.

POST-MILKING:
Dip entire teat in Hex-Plus.  Allow to air dry.
If solution in cup becomes visibly dirty.  Then
replenish with Hex-Plus at full strength.  Do
not return unused product to original container.
PROTECT FROM FREEZING
IF FROZEN: SHAKE VIGOROUSLY
AFTER THAWING

WARNING:  CONTAINS CHLORHEXIDINE
GLUCONATE.

Not for human use.
Avoid contamination of food.  Avoid contact
with eyes.  Not for internal use.

OBSERVE LABEL DIRECTIONS

KEEP OUT OF REACH OF CHILDREN!

FIRST AID:
INTERNAL:  If swallowed, do not induce vomiting.
Drink large quantities of water.  See physician immediately.

EYES:  Flush eyes with clear water for 15 minutes.If irritated, obtain medical guidance.
GET MEDICAL ATTENTION IMMEDIATELY.

Hex-Plus

SANITIZING CHLORHEXIDINE TEAT DIP
FORMULATED WITH EMOLLIENTS AND
DERMAL CONDITIONERS

This product, when properly used, is effective as an aid
in reducing the spread of organisms which may cause
mastitis.
Active Ingredient..........1.0% Chlorhexidine Gluconate
Contains 10% Emollient
Lot#:______________________

Exp. Date:___________________

Next Content:________________

Manufactured For:
Tetradyne LLC
PO Box 17003
Reno, NV 89511

Hex-Plus 
teat dip  liquid Product Information Product Type OTC ANIMAL DRUG NDC Product Code (Source) 66399-742 Route of Administration TOPICAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORHEXIDINE GLUCONATE (CHLORHEXIDINE) CHLORHEXIDINE GLUCONATE 1.0 L  in 100 L Inactive Ingredients Ingredient Name Strength GLYCERIN 10 L  in 100 L Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 66399-742-01 3.78 L In 1 JUG None 2 66399-742-02 18.9 L In 1 PAIL None 3 66399-742-03 56.7 L In 1 DRUM None 4 66399-742-04 113.4 L In 1 DRUM None 5 66399-742-05 207.9 L In 1 DRUM None 6 66399-742-06 945 L In 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK None 7 66399-742-07 1039.5 L In 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/10/2001
Labeler - Tetradyne LLC (130969293) Revised: 11/2010Tetradyne LLC

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Hex-Tra

Generic Name: chlorhexidine gluconate liquid
Dosage Form: FOR ANIMAL USE ONLY
Hex-Tra

USE DIRECTIONS:
Use at full strength, do not dilute.

POST-MILKING:
Dip entire teat in Hex-Tra.  Allow to air dry.
If solution in cup becomes visibly dirty.  Then
replenish with Hex-Tra at full strength.  Do
not return unused product to original container.
PROTECT FROM FREEZING
IF FROZEN: SHAKE VIGOROUSLY
AFTER THAWING

WARNING:  CONTAINS CHLORHEXIDINE
GLUCONATE.

Not for human use.
Avoid contamination of food.  Avoid contact
with eyes.  Not for internal use.

OBSERVE LABEL DIRECTIONS

KEEP OUT OF REACH OF CHILDREN!

FIRST AID:
INTERNAL:  If swallowed, do not induce vomiting.
Drink large quantities of water.  See physician immediately.

EYES:  Flush eyes with clear water for 15 minutes.If irritated, obtain medical guidance.
GET MEDICAL ATTENTION IMMEDIATELY.

Hex-Tra

SANITIZING CHLORHEXIDINE TEAT DIP
FORMULATED WITH EMOLLIENTS AND
DERMAL CONDITIONERS

This product, when properly used, is effective as an aid
in reducing the spread of organisms which may cause
mastitis.
Active Ingredient..........0.50% Chlorhexidine Gluconate
Contains an Emollient System
Lot#:______________________

Exp. Date:___________________

Next Content:________________

Manufactured For:
Tetradyne LLC
PO Box 17003
Reno, NV 89511

Hex-Tra 
teat dip  liquid Product Information Product Type OTC ANIMAL DRUG NDC Product Code (Source) 66399-083 Route of Administration TOPICAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORHEXIDINE GLUCONATE (CHLORHEXIDINE) CHLORHEXIDINE GLUCONATE 0.50 L  in 100 L Inactive Ingredients Ingredient Name Strength GLYCERIN 5.0 L  in 100 L Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 66399-083-01 3.78 L In 1 JUG None 2 66399-083-02 18.9 L In 1 PAIL None 3 66399-083-03 56.7 L In 1 DRUM None 4 66399-083-04 113.4 L In 1 DRUM None 5 66399-083-05 207.9 L In 1 DRUM None 6 66399-083-06 945 L In 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK None 7 66399-083-07 1039.5 L In 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/10/2001
Labeler - Tetradyne LLC (130969293) Revised: 11/2010Tetradyne LLC

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Neutra Maxx

Dosage Form: oral gel
ACTIVE INGREDIENTS

ACTIVE INGREDIENT                                      PURPOSE
SODIUM FLUORIDE (NaF) 1.1% (w/v)               ANTICAVITY
INACTIVE INGREDIENTS
DEIONIZED WATER, XYLITOL, POTASSIUM NITRATE, SODIUM CARBOXYMETHYLCELLOSE, GLYCERIN, FLAVORING,SODIUM SACCHARIN, SODIUM PHOSPHATE .

USE

USE: AIDS IN THE PREVENTION OF DENTAL DECAY IN PEDIATRIC PATIENTS AND ADULTS

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.  IF MORE SOLUTION IS ACCIDENTALLY SWALLOWED THAN USED FOR BRUSHING, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

DIRECTIONS

DIRECTIONS:  (UNLESS INSTRUCTED OTHERWISE BY YOUR DENTAL PROFESSIONAL)   
ADULTS AND CHILDREN 6 YEARS AND OLDER:  USE ONCE A DAY AFTER BRUSHING TEETH WITH TOOTHPASTE.  AFTER RINSING, APPLY THIN RIBBON OF GEL TO TEETH WITH TOOTHBRUSH OR MOUTH TRAYS FOR AT LEASE ONE MINUTE.  BEFORE BEDTIME IS BEST.  ADULTS SHOULD EXPECTORATE AFTER USE.  CHILDREN AGES 6-16 SHOULD EXPECTORATE GEL AND RINSE MOUTH THOROUGHLY.  DO NOT EAT OR DRINK FOR 30 MINUTES AFTER USE.

Warnings

WHEN USING THIS PRODUCT DO NOT SWALLOW UNLESS TOLD TO DO SO BY A DENTIST OR PHYSICIAN.

PACKAGE LABEL

Neutra Maxx 5000PPM GEL  REFRESHING MINT FLAVOR
THE MAXIMUM AMOUNT OF FLUORIDE AVAILABLE  1.1% SODIUM FLUORIDE 5% POTASSIUM  NITRATE XYLITOL SLS FREE Rx ONLY.  NET WT 4.3 oz  (120 g)
MANUFACTURED BY MASSCO DENTAL A DIVISION OF DUNAGIN PHARMACEUTICALS  GRAVETTE, AR 72736  THE MEDICINE AVAILABLE EXCLUSIVELY THROUGH YOUR DENTAL OFFICE. 

OTHER INFORMATION: STORE AT ROOM TEMPERATURE   QUESTION? COMMENTS? CALL 1-479-787-5168 M-F 9AM TO 5PM CST

Neutra Maxx 5000 
sodium fluoride  gel Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 63783-504 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM FLUORIDE (FLUORIDE ION) SODIUM FLUORIDE 1.428 g  in 120 g Inactive Ingredients Ingredient Name Strength WATER   XYLITOL   POTASSIUM NITRATE   CARBOXYMETHYLCELLULOSE SODIUM   GLYCERIN   SODIUM PHOSPHATE   SACCHARIN SODIUM DIHYDRATE   Product Characteristics Color      Score      Shape Size Flavor MINT (Mint) Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 63783-504-06 120 g In 1 BOTTLE, DISPENSING None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part355 01/01/1989
Labeler - Massco Dental A Division of Dunacin Pharmaceuticals (008081858) Registrant - Massco Dental A Division of Dunacin Pharmaceuticals (008081858) Establishment Name Address ID/FEI Operations Massco Dental A Division of Dunacin Pharmaceuticals 008081858 manufacture Revised: 10/2011Massco Dental A Division of Dunacin Pharmaceuticals

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La Vaquita Extra Strength

Dosage Form: ointment
Drug Facts Active Ingredient
Methyl Salicylate 12% Menthol 3% Camphor 2% Eucalyptus Oil 1%
Pain Reliever Pain Reliever Pain Reliever Pain Reliever Uses Provides temporary relief from minor aches and pains associated with back-aches, arthritis, sore aching and strained muscles and joints.
Warnings ? External use only.  Avoid Contact with eyes mucous membranes and broken or irritated skin. Do not swallow. Do not use if allergic to salicylates.  Do not bandage. Do not apply external heat to the application area. Keep away from reach of children

Stop use and ask a doctor if:
pain persists or irritation develops.
Directions Apply generously and gently massage affected area. Repeat 3 times daily. For children under 2 years of age consult a physician.
    
Inactive Ingredients Petrolatum, Paraffin, Lanolin, D and C Red 17.

LA VAQUITA  EXTRA STRENGTH
methyl salicylate  ointment Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 61734-090 Route of Administration TOPICAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (MENTHOL) MENTHOL 3 g  in 100 g Methyl Salicylate (Methyl Salicylate) Methyl Salicylate 12 g  in 100 g CAMPHOR (SYNTHETIC) (CAMPHOR (SYNTHETIC)) CAMPHOR (SYNTHETIC) 2 g  in 100 g EUCALYPTUS OIL (EUCALYPTUS OIL) EUCALYPTUS OIL 1 g  in 100 g Inactive Ingredients Ingredient Name Strength PETROLATUM 75 g  in 100 g PARAFFIN 7 g  in 100 g LANOLIN 0.001 g  in 100 g D&C RED NO. 17 0.0021 g  in 100 g Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 61734-090-01 90 g In 1 CAN None 2 61734-090-02 100 g In 1 JAR None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part348 11/07/2010
Labeler - Delon Laboratories (1990) Ltd (248364184) Establishment Name Address ID/FEI Operations Delon Laboratories (1990) Ltd 248364184 label, manufacture, pack Revised: 11/2010Delon Laboratories (1990) Ltd

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Teat Dip HP 5

Dosage Form: FOR ANIMAL USE ONLY

FOR COMMERCIAL USE ONLY

KEEP OUT OF REACH OF CHILDREN

NOT FOR HUMAN USE

CAUTION

CAUTION

Harmful if swallowed, eye irritant.

FIRST AID :

Avoid contact with skin and eyes. Contact can cause severe irritation. Get medical attention. If ingested, drink large amounts of water or milk. DO NOT induce vomiting. Get immediate attention. Avoid repeated contact with skin and hands. Use rubber gloves to avoid skin irritation. If contact occurs, wash thoroughly with clean water.

EMERGENCY : CHEMTREC 800-424-9300

Prior to milking, dip teats in undiluted Teat Dip HP 5. Wipe off with a clean towel after 15-30 seconds. After milking reapply Teat Dip HP 5. Do not rinse or wash off. Allow teats to dry before letting cows outdoors in cold weather to guard against.

PRINCIPAL DISPLAY PANEL/REPRESENTATIVE LABEL

Teat Dip HP 5

Non-Iodine Teat Dip

An Aid Reducing the Spread of Organisms

Which May Cause Mastitis

ACTIVE INGREDIENTS:

Hydrogen Peroxide........................0.5%

INACTIVE INGREDIENTS............99.5%

Wausau Chemical Corporation

2001 North River Drive

Wausau, WI 54403-0953 U.S.A.

Teat Dip HP 5 
hydrogen peroxide  solution Product Information Product Type OTC ANIMAL DRUG NDC Product Code (Source) 64892-006 Route of Administration TOPICAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Hydrogen Peroxide (Hydrogen Peroxide) Hydrogen Peroxide 0.5 L  in 100 L Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 64892-006-16 18.9 L In 1 DRUM None 2 64892-006-17 56.78 L In 1 DRUM None 3 64892-006-18 113.6 L In 1 DRUM None 4 64892-006-21 208.2 L In 1 DRUM None 5 64892-006-88 1040 L In 1 CONTAINER None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/15/2010
Labeler - Wausau Chemical Corporation (006136220) Establishment Name Address ID/FEI Operations Wausau Chemical Corporation 006136220 manufacture Revised: 06/2010Wausau Chemical Corporation

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Petco Iodoform

Dosage Form: FOR ANIMAL USE ONLY
Product facts Directions

Hold application tip one inch from ear canal. Squeeze PETCO Ear Powder directly into the ear. In severe cases treat daily. Weekly application will help keep your pet's ears in good condition.
PETCO Ear Powder may also be used in removing excess ear hair. Applying powder into the ear makes hair  easier to grip and minimizes irritation caused by hair removal. Use regularly with PETCO Ear Cleansing Wipes or PETCO Ear Cleansing Liquid to maintain good ear health.

Active Ingredient

5% Iodoform in an inert base.

Inactive Ingredient

Talc

Warning

Keep this product out of reach of children and pets to prevent unintended consumption

For Questions Call 1-877-473-8465

ear Pwder

PETCO Ear Powder gives prompt relief from irritated, itching ears of non-parasitic origin. It stops scratching and aids in the inhibition of bacterial growth. Eliminates unpleasant ear odors. PETCO Ear Powder dries ear discharge and makes it easy to remove. For topical use within the ears of dogs.

PETCO

EAR

POWDER

For Dogs

provides relief from itching and irritation Helps keep dog's ears dry, clean and healthy Fast acting formula NET WT. 1 OZ. (28g)
PETCO 
iodoform  powder Product Information Product Type OTC ANIMAL DRUG NDC Product Code (Source) 27102-810 Route of Administration TOPICAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IODOFORM (IODOFORM) IODOFORM 1.4 g  in 28 g Inactive Ingredients Ingredient Name Strength TALC   Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 27102-810-08 1 BOX In 1 BOX contains a BOTTLE (27102-810-15) 1 27102-810-15 28 g In 1 BOTTLE This package is contained within the BOX (27102-810-08)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/01/2001
Labeler - Petco (028364727) Registrant - United Pet Group (931135730) Establishment Name Address ID/FEI Operations JUNGLE LABORATORIES CORPORATION 032615270 manufacture Revised: 02/2010Petco

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Nucleoside reverse transcriptase inhibitors (NRTIs)

A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

Nucleoside reverse transcriptase inhibitors (NRTIs) are active inhibitors of reverse transcriptase found in retroviruses such as the human immunodeficiency virus (HIV). The different nucleoside reverse transcriptase inhibitors may be activated differently but they have the same mechanism of action. NRTIs are activated generally by phosphorylation to the triphosphate form by cellular enzymes. It then competes with cellular triphosphates, which are substrates for proviral DNA by viral reverse transcriptase. NRTI

See also

Medical conditions associated with nucleoside reverse transcriptase inhibitors (NRTIs):

Hepatitis B HIV Infection Nonoccupational Exposure Occupational Exposure Reduction of Perinatal Transmission of HIV Drug List: Baraclude Hepsera Videx-Chewable-Dispersible-Buffered-Tablets Viread Ziagen Epivir Retrovir Zerit Emtriva Epivir-Hbv Hivid Tyzeka Videx-Ec-Delayed-Release-Enteric-Coated-Capsules

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Sentry HC Worm X

Dosage Form: FOR ANIMAL USE ONLY
Broad Spectrum De-Wormer Chewable Tablets for Large Dogs INDICATIONS & USAGE

For Removal of Hookworms in Puppies and Dogs

Ancylostoma caninum Uncinaria stenocephala For Removal of Large Roundworms (Ascarids) in Puppies and Dogs
Toxocara canis Toxascaris leonina To Prevent Reinfection of Large Roundworms in Puppies, Adult Dogs and Lactating Bitches After Whelping
Toxocara canis ACTIVE INGREDIENT (in each chewable) Pyrantel Pamoate (113.5 mg) How is Sentry HC Worm X Supplied Net Contents:    2 Tablet Count
Net Contents:    4 Tablet Count
Net Contents:  12 Tablet Count STORAGE Store at controlled room temperature of 59-86 degrees F (15-30 degrees C). PACKAGE LABEL PRINCIPAL DISPLAY PANEL Sentry HC Worm X
Distributed by:
Sergeant's Pet Care Products, Inc., Omaha NE 68130
www.sentrypetcare.com
ANADA #200-281, Approved by FDA
Sentry HC Worm X 
pyrantel pamoate  tablet, chewable Product Information Product Type OTC ANIMAL DRUG NDC Product Code (Source) 21091-402 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRANTEL PAMOATE (PYRANTEL) PYRANTEL PAMOATE 113.5 mg Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color brown Score no score Shape ROUND Size 10mm Flavor LIVER (Pork Liver Powder) Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 21091-402-02 1 BLISTER PACK In 1 CARTON contains a BLISTER PACK 1 2 TABLET In 1 BLISTER PACK This package is contained within the CARTON (21091-402-02) 2 21091-402-04 2 BLISTER PACK In 1 CARTON contains a BLISTER PACK 2 4 TABLET In 1 BLISTER PACK This package is contained within the CARTON (21091-402-04) 3 21091-402-12 6 BLISTER PACK In 1 CARTON contains a BLISTER PACK 3 12 TABLET In 1 BLISTER PACK This package is contained within the CARTON (21091-402-12)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANADA ANADA200281 01/16/2008
Labeler - Sergeant's Pet Care Products, Inc. (876995171) Establishment Name Address ID/FEI Operations Virbac Bridgeton 808558100 manufacture Revised: 11/2010Sergeant's Pet Care Products, Inc.

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Sentry HC Worm X

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