Active Ingredient
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 71011-005
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 71011-005). 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.
Flammable: Keep away from flame or high heat
When using this product keep out of eyes.In case of contact flush eyes with water. Avoid contact with broken skin.
Stop use and ask a doctor if irritation or redness develop.
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
Rub hands thoroughly with product and allow to dry.
Inactive Ingredient
Water, Glycerin, Propylene Glycol, Carbomer, Triethanolamine, Fragrance, FD&C BLUE NO.1
Package Label.Principal Display Panel
1 (1)
2 (2)
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