AMBI Soothing Hand sanitizer
AMBI Soothing Hand sanitizer is an FDA drug label for the active ingredient ALCOHOL manufactured by AMBI Enterprises, 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 20231105.
Generic: ALCOHOL
Manufacturer: AMBI Enterprises, llc
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 73453-143
Application: 505G(a)(3)
Effective: 20231105
Active Ingredients: Active ingredient Ethyl Alcohol 70% Purpose Topical Antimicrobial
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. Flammable. Keep away from heat or flame. Do not use in children less than 2 months of age on 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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