AntiochPharma Hand Sanitizer
AntiochPharma Hand Sanitizer is an FDA drug label for the active ingredient ALCOHOL manufactured by Weeks & Leo 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 20231211.
Generic: ALCOHOL
Manufacturer: Weeks & Leo
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 11383-308
Application: M003
Effective: 20231211
Active Ingredients: Active Ingredients Alcohol 70% v/v..................................................................Antiseptic
Indications & Usage
Uses hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Dosage & Administration
Directions Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing
Contraindications
Not available.
Warnings
Warnings For external use only Do not use in children less than 2 months of ageon open skin wounds When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Stop use and ask a doctor if Irritation or rash occurs. These may be signs of a serious condition. Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away
Adverse Reactions
Not available.
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