Active Ingredient(S)
Ethyl Alcohol 62% v/v
Hand Sanitizer
FDA Label NDC 76681-012
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Taizhou Huangyan Delishi Daily Necessity Co., Ltd. for the product Hand Sanitizer (NDC 76681-012). 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(s), purpose, use, do not use, otc - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
To help reduce bacteria and germs on the skin
Do Not Use
In children less than 2 month of age. On open skin wounds
Otc - When Using
/
Otc - Stop Use
If irritation or rash occurs. These may be signs of a serious condition.
Otc - Keep Out Of Reach Of Children
If swallowed, get medical hep or contact a Poison Control Center right away.
Directions
Place enough product in palm to cover hands and Rub hands together briskly until dry.
Children under 6,use only under adult suoervision.
Not recommended for infants.
Inactive Ingredients
Water (Aqua), Carbomer, Glycerol, Triethanolamine(TEA), Fragrance
Package Label - Principal Display Panel
61 (43461)
52 (43452)
53 (43453)
57 (43457)
64 (43464)
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