Ethyl Rubbing Alcohol
Ethyl Rubbing Alcohol is an FDA drug label for the active ingredient ALCOHOL manufactured by Humco Holding Group, Inc. administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231215.
Generic: ALCOHOL
Manufacturer: Humco Holding Group, Inc.
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 0395-0040
Application: M003
Effective: 20231215
Active Ingredients: Active Ingredient Ethyl Alcohol 70% by volume
Indications & Usage
Use First aid to help prevent the risk of infection in. minor cuts scrapes burns
Dosage & Administration
Directions clean the affected area. apply a small amount of this product on the affected area 1 to 3 times daily. may be covered with sterile bandage. if bandaged, let it dry first.
Contraindications
Not available.
Warnings
Warnings For external use only. Flammable, keep away from spark, heat and flame.
Adverse Reactions
Not available.
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