Active Ingredient
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 71011-003
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 71011-003). 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 & around eyes
When using this product
■Keep away from fire or flame
■Using other topical acne drugs at the same time or right after use of this product may increase dryness or irritation of the skin . Only one drug should be used unless directed by a doctor.
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 onto hands and rub hands and rub hands together briskly until dry
Inactive Ingredient
Deionized Water, glycerin , Propylene Glycol, aloe vera gel,fragrance,DMDMH
Package Label.Principal Display Panel
1 (Label)
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