Alcohol Prep
Alcohol Prep is an FDA drug label for the active ingredient ISOPROPYL ALCOHOL manufactured by Topco Associates 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 20231227.
Generic: ISOPROPYL ALCOHOL
Manufacturer: Topco Associates
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 76162-809
Application: M003
Effective: 20231227
Active Ingredients: Active ingredient Isopropyl Alcohol, 70% v/v
Indications & Usage
Uses First aid to decrease germs in minor cuts, scrapes and burns.
Dosage & Administration
Directions Apply to skin as needed Discard after single use
Contraindications
Not available.
Warnings
Warnings For external use only. Flammable. Keep away from fire or flame. Do not use with electrocautery procedures longer than 1 week unless directed by a doctor When using this product do not get into eyes do not apply over large areas of the body in case of deep or puncture wounds, animal bites or serious burns, consult a doctor Stop use and ask a doctor if irritation and redness develop condition gets worse or persists for more than 72 hours Keep out of reach of children. If accidentally swallowed, get medical help or contact a Poison Control Center right away.
Adverse Reactions
Not available.
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