Animal NDC 57932-005-01 Oinkment
Ethyl Alcohol, Sodium Propionate

Animal Product Information

Field Name Field Value
Animal NDC Code 57932-005-01
Proprietary Name Oinkment What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name Ethyl Alcohol, Sodium Propionate What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
Labeler Name Animal Science Products, Inc.
Product Type Otc Animal Drug
Usage Information
    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.
Active Ingredient(s)
  • Alcohol
  • Sodium Propionate
Inactive Ingredient(s)
  • WATER (059QF0KO0R)
  • ANHYDROUS CITRIC ACID (XF417D3PSL)
  • METHYLCELLULOSE, UNSPECIFIED (Z944H5SN0H)
  • FD&C YELLOW NO. 5 (I753WB2F1M)
  • FD&C BLUE NO. 1 (H3R47K3TBD)
  • WATER (059QF0KO0R)
  • ANHYDROUS CITRIC ACID (XF417D3PSL)
  • METHYLCELLULOSE, UNSPECIFIED (Z944H5SN0H)
  • FD&C YELLOW NO. 5 (I753WB2F1M)
  • FD&C BLUE NO. 1 (H3R47K3TBD)
Marketing Category UNAPPROVED DRUG OTHER What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Oinkment Animal Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



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


Inactive Ingredient



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


Product Label



Bottle Label


* The information on this page is for an ANIMAL PRODUCT, please review the complete disclaimer below.