Oinkment: Product Information

OINKMENT- alcohol and sodium propionate liquid
Animal Science Products, Inc.

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.

Active Ingredient

Ethyl Alcohol…………………………………72.6%
Sodium Propionate………………………….0.5%

Purpose

QUICK-DRYING ANTIMICROBIAL FLEXIBLE FILM BANDAGE

FOR VETERINARY USE ONLY

Uses

For use as a topical microbiocidal barrier on the skin of swine to shield from abrasion and guard against contamination that may cause infection

Warnings

  • For external use only.
  • Store at room temperature.
  • Not for human use.
  • Keep out of reach of children.

Directions

Shake well before use. For best results, clean and dry the wound and surrounding skin for good adhesion. Apply Oinkment with spray tip 6 inches from wound, spraying to completely cover the wound and overlap onto surrounding healthy skin.

Reapply every other day or as required to keep the wound sealed until satisfactory.

ADVANTAGES


• Easy to spray, dries fast to form a flexible film bandage for abrasions, cuts and scrapes
• Covers and seals wound to maintain clean, moist healing environment
• Antibacterial and antifungal activity
• Deters tail biting
• Soothing analgesic action
• Highly visible
• Safe, non-toxic, 100% GRAS (21 CFR) food approved components
• No preslaughter withdrawal required
• Removal and cleanup with water

Keep Out Of reach of Children

Inactive Ingredient

Anhydrous citric acid, Water, FD&C yellow no. 5, FD&C blue no. 1, Methylcellulose

Product Label

Bottle Label

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Box Label

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OINKMENT
ethyl alcohol, sodium propionate liquid
Product Information
Product Type OTC ANIMAL DRUG Item Code (Source) NDC:57932-005
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 7.2 mg in 1 mL
SODIUM PROPIONATE (PROPIONIC ACID) SODIUM PROPIONATE 0.5 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
ANHYDROUS CITRIC ACID
METHYLCELLULOSE, UNSPECIFIED
FD&C YELLOW NO. 5
FD&C BLUE NO. 1
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:57932-005-01 12 BOTTLE in 1 BOX contains a BOTTLE
1 1000 mL in 1 BOTTLE This package is contained within the BOX (57932-005-01)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 05/14/2020
Labeler — Animal Science Products, Inc. (151824091)
Establishment
Name Address ID/FEI Operations
Animal Science Products, Inc. 151824091 manufacture, api manufacture

Revised: 05/2020 Animal Science Products, Inc.

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