Active Ingredient
Ethyl Alcohol 70%
Amerigel Hand Sanitizer
FDA Label NDC 61470-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Amerx Health Care Corp for the product Amerigel Hand Sanitizer (NDC 61470-001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, do not use, when using this product, stop use and ask a doctor., keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
For handwashing to decrease bacteria on skin when soap and water are not available.
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 immediately.
Directions
Wet hands thoroughly with product. Rub hands together briskly until dry. Supervise children under 6 years of age when using this product.
Other Information
Store below 110F (43C)
Inactive Ingredients
Water, Aloe Barbadensis, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Propylene Glycol, PEG-8 Dimethicone, Triisopropanolamine, Linalool, FD&C Blue #1
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