Freeman Packaging Hand Sanitizer
Freeman Packaging Hand Sanitizer is an FDA drug label for the active ingredient ALCOHOL manufactured by JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD. 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 20171009.
Generic: ALCOHOL
Manufacturer: JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 71734-201
Application: part333E
Effective: 20171009
Active Ingredients: Active Ingredient Ethyl Alcohol 62% Purpose antiseptic
Indications & Usage
Uses to decrease bacteria on the skin that could cause disease recommended for repeated use
Dosage & Administration
Directions wet hands thoroughly with product and allow to dry without wiping for children under 6, use only under adult supervision not recommended for infants
Contraindications
Not available.
Warnings
Warnings For external use only- hands. Flammable. Keep away from heat and flame. When using this product, keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest. Stop use and ask a doctor if skin irritation develops. When using this product keep out of eyes. In case of contact with eyes, immediately flush with water and call a doctor. avoid contact with broken skin. Stop use and ask a doctor if skin irritation develops Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.
Adverse Reactions
Not available.
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