Active Ingredient
Ethyl Alcohol 70%
Hand Sanitizer
FDA Label NDC 74649-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Yiwu Pharmacy Ecomm Business Enterprise Ltd for the product Hand Sanitizer (NDC 74649-000). 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:, other, when using this product, stop use and ask a doctor if, 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
Antimicrobial
Uses:
- A hand sanitizer to help reduce bacteria on the skin
Warnings:
For External Use Only.
Other
Flammable. Keep away from fire or flame or sparks
When Using This Product
do not use in or near eyes. In case of contact, rinse eyes thoroughly with water.
Stop Use And Ask A Doctor If
irritation or rash appears on the skin
Keep Out Of Reach Of Children.
If swallowed, get immediate help or contact a Poison Control Center right away.
Directions:
- Place enough to cover both hands in the palm, and rub hands together until dry.
- Children under 6 years of age should be supervised by adult when applying this product.
Other Information.
- Store below 110 oF (43 oC)
- May discolor certain fabrics or surfaces.
Inactive Ingredient
Purified water, Carbomer 940, PEG12 - dimethicone, Propylene glycol, Aloe barbadensis leaf extract, Triethanolamine, Fragrance
Package Labeling: 74649-000-02
59ml (59ml)
Package Labeling:74649-000-08
236ml (236ml)
Package Labeling:74649-000-01
Label (Label)
Package Labeling:74649-000-16
Label2 (Label2)
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