Label: PROVITA EQUIBAND- benzoic acid spray
- NDC Code(s): 16371-105-01, 16371-105-02, 16371-105-03
- Packager: Provita Eurotech Ltd
- Category: OTC ANIMAL DRUG LABEL
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Drug Label Information
Updated December 17, 2018
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- Official Label (Printer Friendly)
- DESCRIPTION
- SPL UNCLASSIFIED SECTION
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PRECAUTIONS
Danger: Flammable liquid and vapour. Harmful if swallowed. Keep away from heat/ sparks/open flames/hotsurfaces — No smoking. 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 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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DOSAGE & ADMINISTRATION
Directions for Use
For use topically on hooves and all skin types (except face). Clean and dry the area carefully before use. Spray an even coating and allow 1-2 minutes for the film to form.
For hoof areas, ensure that the film is formed before returning the hoof to the ground. Where necessary, repeat application every 2 days for up to 10 days.
- PRINCIPAL DISPLAY PANEL - 500 ml Bottle Label
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INGREDIENTS AND APPEARANCE
PROVITA EQUIBAND
benzoic acid sprayProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:16371-105 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Benzoic acid (UNII: 8SKN0B0MIM) (Benzoic acid - UNII:8SKN0B0MIM) Benzoic acid 74 g in 1 L Product Characteristics Color ORANGE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:16371-105-01 0.5 L in 1 BOTTLE, SPRAY 2 NDC:16371-105-02 1 L in 1 BOTTLE, SPRAY 3 NDC:16371-105-03 0.25 L in 1 BOTTLE, SPRAY 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 MANUFACTURE, PACK, LABEL, ANALYSIS, API MANUFACTURE