Otc - Active Ingredient
Active ingredient Purpose
Ethyl Alcohol 70% ... Antiseptic
Aurafresh Instant Hand Sanitizer
FDA Label NDC 40104-284
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Pulisi Daily Chemical Products Co., Ltd. for the product Aurafresh Instant Hand Sanitizer (NDC 40104-284). 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, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Hand sanitizer to help decrease bacteria on the skin.
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact local poison control center right away.
Children under 6 years of age should be supervised when using this product.
Indications & Usage
keep out of eyes
when water, soap and towel are not available
Warnings
For external use only.
Flammable. Keep away from hear or flame.
When using this products, do not use in or the eyes. In case of contact, rinse eyes thoroughly with water.
Stop using and ask a doctor, if irritation or rash appears and lasts.
Dosage & Administration
place enough product in your palms to thoroughly spread on both hands, and rub into the skin until dry.
Inactive Ingredient
Water, Carbomer, Glycerin, Propylene Glycol, Triethanolamine, acrylates/c10-30 alkyl acrylate crosspolymer, isopropyl alcohol, aminomethyl propanol, isopropyl mysistate, caprylyl glycol, phenoxyethanol, Tocopheryl Acetate, Fragrance
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