Label: ISOPROPYL ALCOHOL- isopropyl alcohol liquid
- NDC Code(s): 30798-786-35
- Packager: Durvet, Inc.
- 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 30798-786-35 durvet 70% ALCOHOL SOLUTION Contains 70% Isopropyl Alcohol
- FOR ANIMAL USE ONLY
INDICATIONS: Helps relieve minor muscular aches due to overexertion.
DIRECTIONS: Apply liberally and rub in.Close
Harmful if swallowed.Close
FOR EXTERNAL USE ONLY. Keep out of reach of children. If taken internally, severe gastric disturbances will result. In case of accidental ingestion, call a physician or poison control center immediately. Causes eye irritation. In case of contact, immediately flush eyes with water and call a physician. May cause skin irritation. Avoid contact with eyes, skin, mucous membranes and clothing. Wash hands thoroughly after handling.
TAKE TIME OBSERVE LABEL DIRECTIONS
Blue Springs, Missouri 64014
- KEEP OUT OF REACH OF CHILDREN
Isopropyl Alcohol ................ 70%
Purified Water .................... 30%
This preparation is made from Isopropyl Alcohol and does not contain, nor is it sold as a substitute for, ethyl or grain alcohol.Close
Store at controlled room temperature between 15º - 30ºC (59º-86ºF). Keep tightly closed, protect from light.Close
- WARNING! FLAMMABLE!
KEEP AWAY FROM HEAT AND OPEN FLAME
Lot No. Exp. DateClose
- INGREDIENTS AND APPEARANCE
isopropyl alcohol liquid
Product Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:30798-786 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 70 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:30798-786-35 3785 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved drug other 08/10/2009 Labeler - Durvet, Inc. (056387798)