sunmark Isopropyl Rubbing Alcohol

sunmark Isopropyl Rubbing Alcohol is an FDA drug label for the active ingredient ISOPROPYL ALCOHOL manufactured by Strategic Sourcing Services LLC 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 20231219.

Generic: ISOPROPYL ALCOHOL

Manufacturer: Strategic Sourcing Services LLC

Product Type: HUMAN OTC DRUG

Route: TOPICAL

Dosage Form:

NDC: 49348-030

Application: M003

Effective: 20231219

Active Ingredients: Active Ingredient Isopropyl Alcohol 70% U.S.P. by volume

Indications & Usage

Uses First aid to help prevent infection in minor cuts, scrapes, and burns. For rubbing massage and as an external stimulant.

Dosage & Administration

Directions For antiseptic use: Apply a small amount of this product to the affected area 1 to 3 times daily. May be covered with sterile bandage. If bandaged let dry first. For rubbing or massage use: Apply compound externally on body until liquid has been absorbed or has been evaporated.

Contraindications

Not available.

Warnings

Warnings For External use only. USE IN WELL VENTILATED AREA. FUMES MAY BE HARMFUL. Do not use in the eyes or apply over a large area of the body when used as an antiseptic. In case of deep or puncture wounds, animal bites, or serious burns, consult a doctor. When using this product: Do not apply to irritated skin and avoid getting into eyes or mucous membranes. Stop use and consult a doctor if the condition persists or gets worse. Do not use longer than 1 week unless directed by a doctor. Discontinue use if excessive irritation of the skin develops. Keep out of reach of children. In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately. In case of eye contact, flush eyes with running water for 15 minutes.

Adverse Reactions

Not available.

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