Active Ingredient
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 76897-001
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 Laiao Daily Chemical Co, Ltd. for the product Hand Sanitizer (NDC 76897-001). 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, warnings, otc - keep out of reach of children, directions, inactive ingredients, 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
Warnings
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.
Stop use and ask a doctor if rash occurs
Otc - 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 Ingredients
Deionized Water, Carbomer， Triethanolamine,Aloe
barbadensis Gel,Fragrance ，Glycerin, Propylene Glycol,
Vitamin E
Package Label.Principal Display Panel
1 (Label)
* Please review the disclaimer below.
