Label: ISOPROPYL ALCOHOL- isopropyl alcohol liquid
- NDC Code(s): 50989-492-27
- Packager: Vedco
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
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- NDC 50989-492-27 ISOPROPYL ALCOHOL 99% LIVESTOCK DRUG NET CONTENTS: 32 fl. oz.
KEEP AWAY FROM FIRE OR FLAME
KEEP OUT OF REACH OF CHILDRENClose
- For Animal Use Only
To make a standard solution:
Dilute with 30% water to 70% alcohol. Scrub hands and arms with soap and water, rinse with water, then scrub with alcohol solution for disinfecting.
External Solution: For use as a topical antispectic. May also be used for temporary relief of minor muscular aches or pain due to overexertion and fatigue. Apply full strength directly to afflicted area, wet thoroughy and massage briskly to stimulate circulation.Close
- Store at controlled room temperature between 15° and 30°C (59°F-86°F).
TAKE TIME OBSERVE LABEL DIRECTIONS
St. Joseph, MO 64504Close
- ACTIVE INGREDIENT:
- INERT INGREDIENT:
For external use only. If taken internally, serious gastric disturbance will result. Avoid contact with eyes. In case of eye contact, flush thoroughly with water. Call a physician.
First Aid: Induce vomiting or use stomach pump.
FLAMMABLE: Do not use near heat or open flame.
Lot No. Exp. Date
- PRINCIPAL DISPLAY PANEL
IPA Bottle Label
- INGREDIENTS AND APPEARANCE
isopropyl alcohol liquid
Product Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:50989-492 Route of Administration TOPICAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 99 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50989-492-27 946 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved drug other 04/12/1999 Labeler - Vedco (021634266)