ISOPROPYL ALCOHOL

ISOPROPYL ALCOHOL is an FDA drug label for the active ingredient ISOPROPYL ALCOHOL manufactured by Degasa, S.A. de C.V. 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 20231105.

Generic: ISOPROPYL ALCOHOL

Manufacturer: Degasa, S.A. de C.V.

Product Type: HUMAN OTC DRUG

Route: TOPICAL

Dosage Form:

NDC: 67326-035

Application: 505G(a)(3)

Effective: 20231105

Active Ingredients: Active Ingredient Isopropyl alcohol 91% Purpose First Aid Antiseptic

Indications & Usage

Uses 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 product on the area 1 o 3 times daily May be covered with a sterile bandage. If bandaged, let dry first.

Contraindications

Not available.

Warnings

Warnings For external use only Flammable Keep away from fire or flame, heat, spark, electrical Ask a doctor before use if you have deep or puncture wounds, animal bites or serious burns When using this product Do not get into eyes Do not inhale Do not apply over large areas of the body Do not use longer than 1 week Stop use and ask a doctor if condition persists or gets worse Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Caution Fumes can be acutely irritating to skin, eyes and the respiratory system. Do not apply to irritated skin or if excessive irritation develops. Avoid getting into the eyes or on mucous membranes. Avoid inhaling this product.

Adverse Reactions

Not available.

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