AP HanSan
AP HanSan is an FDA drug label for the active ingredient ALCOHOL manufactured by WhiskProducts, 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 20231207.
Generic: ALCOHOL
Manufacturer: WhiskProducts, Inc.
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 65585-580
Application: 505G(a)(3)
Effective: 20231207
Active Ingredients: Active Ingredient Ethyl Alcohol 60% v/v
Indications & Usage
Use To help reduce the amount of bacteria on the skin
Dosage & Administration
Directions Place a small amount of spray into the hands. Spread on hands and rub into skin until dry. Place a smaller amount in one hand and spread over both hands and wrists. Rub into skin until dry. Children should be supervised while using this product.
Contraindications
Not available.
Warnings
Warnings Flammable. Keep away from fire or flame. For external use only. If swallowed seek medical attention. When using this product do not use around or near the eyes. If contact occurs, flus eyes iwth water and contact doctor immediately. Stop use and consult a doctor when skin irritation appears and lasts. Keep out of reach of children.
Adverse Reactions
Not available.
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