Otc - Active Ingredient
Active ingredient
Alcohol, 62% v/v
Aosi Healthcare Hand Sanitizer Gel
FDA Label NDC 43473-056
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nantong Health & Beyond Hygienic Products Inc. for the product Aosi Healthcare Hand Sanitizer (NDC 43473-056). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - keep out of reach of children, dosage & administration, storage and handling, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose Antiseptic
Indications & Usage
Uses
- For hand sanitizing to decrease bacteria on the skin without soap and water
Warnings
Warnings
For external use only.
Flammable, keep away from heat or flames
Otc - Do Not Use
Do not use in the eyes
Use with caution if allergic to alcohol
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center directly.
Dosage & Administration
Directions:
• Put enough product on your palm to cover hands and briskly rub hands together until dry.
• For children under 6 years old, use only under adult supervision.
Storage And Handling
Other information
- Storage below 105°F.
- May discolor some fabrics.
- Harmful to wood finishes and plastic
Inactive Ingredient
Inactive ingredients
Acrylates/C10-30 alkyl acrylate crosspolymer, Aloe barbadensis leaf juice, Fragrance, Glycerin, Maltodextrin, Propylene glycol, Tocopheryl acetate,
Triethanoamine, Water
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