Active Ingredient
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 71011-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Huize Commodity Co.,ltd. for the product Hand Sanitizer (NDC 71011-001). 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, use, warning, keep out of reach of children, directions, 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
Purpose
Antiseptic
Use
Decreases bacteria on hands
Warning
for external use only
Do not use
on broken skin
on large areas of the body
Keep Out Of Reach Of Children
Keep out of reach of children
If swallowed ,get medical help or contact a Poison on Control Center immediately
Directions
Squeeze ont oh ands and rub hands and rub hands together briskly until dry
Can be used anytime any place, without water or towels
Contains moisturizers and vitamin E to leave hands feeling refreshed ,soft and smooth without stickiness or residue.
Inactive Ingredient
Deionized Water, Carbomer ,Triethanolamine, Aloe barbadensis Gel, Fragrance Glycerin,
Propylene Glycol,Vitamin E
* Please review the disclaimer below.
