Sanix Alcohol Hand Rub
Sanix Alcohol Hand Rub is an FDA drug label for the active ingredient ALCOHOL manufactured by Topiderm, 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 20200324.
Generic: ALCOHOL
Manufacturer: Topiderm, Inc
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 51326-900
Application: M003
Effective: 20200324
Active Ingredients: Active ingredients Ethyl Alcohol 62% (v/v)
Indications & Usage
Uses Hand sanitizer for reduction of bacteria on the skin.
Dosage & Administration
Directions Apply enough product into the palm and rub hands together to thoroughly wet them Continue until the product dries without wiping off Supervise children when they are using the product Store below 110°F (43°C) May discolor some types of fabrics & surfaces.
Contraindications
Not available.
Warnings
Warnings For external use only. Flammable. Keep away from fire and flame. Keep out of and away from the eyes. In case of eye contact flush thoroughly with water. Stop use and ask a doctor if irritation or rash appears and lasts. Keep out of reach of children. Not for use on infants. If product is swallowed, get medical help or contact a Poison Control Center immediately.
Adverse Reactions
Not available.
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