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
- 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 December 18, 2018
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
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SPL UNCLASSIFIED SECTION
A proprietary blend of organic acids and essential oils with potent penetrating action. Does not contain copper or antibiotics. 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. Ingredients: Organic acids (Acetic, Formic and Salicylic), Pyrrolidone, Water, Hydroxyethylcellulose, Tea-tree Oil, Ethanol, Alkoxylated Cetyl Alcohol, Laureth-4, E124, E133
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PRECAUTIONS
Danger: Flammable liquid and vapour. Harmful if swallowed. Causes severe skin burns and eye damage. Keep away from heat/ sparks/open flames/hot surfaces — No smoking. Toxic if inhaled. May damage the unborn child. Care must be taken when handling product . Do not breathe dust / fume / gas / mist / vapours / spray. Wear protective gloves/ protective clothing/eye protection/face protection. IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing.
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DOSAGE & ADMINISTRATION
Rinse skin with water/ shower. IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do, continue rinsing. If symptoms persist, immediately call a POISON CENTER or doctor/physician. In case of fire: Use water, carbon dioxide (CO2), foam, dry powder for extinction. Store in a well-ventilated place. Keep cool. Keep out of reach of children. For animal use only.
- 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 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