Label: PROVITA KONQUEST- formic acid gel
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NDC Code(s):
16371-104-01,
16371-104-02,
16371-104-03,
16371-104-04, view more16371-104-05, 16371-104-06, 16371-104-07, 16371-104-08, 16371-104-09
- Packager: Provita Eurotech Ltd
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated August 11, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- VETERINARY INDICATIONS
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Directions for Use
For use in sheep, cattle, horses and goats. Clean and dry hooves thoroughly before use. Pare hoof, if necessary. Apply the gel to the affected area using a standard caulking gun. Wipe end of the nozzle with a clean cloth and replace cap tightly after each use. Can be used with a hoof bandage. After a maximum of two days, remove the wrap. Where necessary, repeat application.
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Precautions
Care must be taken when handling product.
Wear suitable protective clothing and eye protection.
Do not breathe vapour.
Contains Formic Acid.
Causes burns.
In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
Keep out of reach of children.
See Health and Safety Data Sheet.
For external use only.
For animal use only.
Keep Cool.
- Ingredients
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 300 g Cartridge Label
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INGREDIENTS AND APPEARANCE
PROVITA KONQUEST
formic acid gelProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:16371-104 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FORMIC ACID (UNII: 0YIW783RG1) (FORMIC ACID - UNII:0YIW783RG1) FORMIC ACID 14.5 g in 100 g Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) CETYL ALCOHOL (UNII: 936JST6JCN) LAURETH-4 (UNII: 6HQ855798J) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) PONCEAU 4R (UNII: Z525CBK9PG) ACETIC ACID (UNII: Q40Q9N063P) TEA TREE OIL (UNII: VIF565UC2G) SALICYLIC ACID (UNII: O414PZ4LPZ) PYRROLIDONE (UNII: KKL5D39EOL) CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X) Product Characteristics Color BLUE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:16371-104-02 48 in 1 CARTON 1 NDC:16371-104-01 300 g in 1 CARTRIDGE 2 NDC:16371-104-04 12 in 1 CARTON 2 NDC:16371-104-03 15 g in 1 SYRINGE, PLASTIC 3 NDC:16371-104-06 12 in 1 CARTON 3 NDC:16371-104-05 30 g in 1 SYRINGE, PLASTIC 4 NDC:16371-104-08 48 in 1 CARTON 4 NDC:16371-104-07 300 g in 1 JAR 5 NDC:16371-104-09 72 in 1 CARTON 5 NDC:16371-104-07 300 g in 1 JAR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED DRUG OTHER 01/01/2012 Labeler - Provita Eurotech Ltd (238318232) Establishment Name Address ID/FEI Business Operations Provita Eurotech Ltd 220688192 API MANUFACTURE, MANUFACTURE, PACK, LABEL, ANALYSIS
