OINKMENT- ethyl alcohol, sodium propionate liquid

Oinkment by

Drug Labeling and Warnings

Oinkment by is a Animal medication manufactured, distributed, or labeled by Animal Science Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

Product label

Box label

INGREDIENTS AND APPEARANCE

OINKMENT 
ethyl alcohol, sodium propionate liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 57932-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	7.2 mg  in 1 mL
SODIUM PROPIONATE (UNII: DK6Y9P42IN) (PROPIONIC ACID - UNII:JHU490RVYR)	SODIUM PROPIONATE	0.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
METHYLCELLULOSE, UNSPECIFIED (UNII: Z944H5SN0H)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57932-005-01	12 in 1 BOX
1		1000 mL in 1 BOTTLE

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	Business Operations
Animal Science Products Inc.		151824091	manufacture

Establishment
Name	Address	ID/FEI	Business Operations
Delta Synthetic Co., Ltd.		656128618	api manufacture