Label: PROVITA KONQUEST- formic acid gel

  • NDC Code(s): 16371-104-01, 16371-104-02, 16371-104-03, 16371-104-04, view more
    16371-104-05, 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.

  • 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.

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  • SPL UNCLASSIFIED SECTION

    Provita Eurotech Limited

    21 Bankmore Road, Omagh,

    Co. Tyrone, Northern Ireland, BT79 0EU Provita Animal Health LLC

    4500 140TH Avenue North,

    Suite 101, Clearwater, FL 33762

    Tel: + (1) 727 431 9511

    Email: info@provita-animalhealth.com www.provita-animalhealth.com

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  • PRINCIPAL DISPLAY PANEL - 300 g Cartridge Label

    Provita
    Animal Health Naturally

    ANTIBIOTIC
    FREE

    Hoofsure
    Konquest

    Topical hoof gel

    30
    Applications

    300g

    PRINCIPAL DISPLAY PANEL - 300 g Cartridge Label
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  • INGREDIENTS AND APPEARANCE
    PROVITA KONQUEST 
    formic acid gel
    Product 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
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