Active Ingredient(S)
Ethyl Alcohol 75% v/v. Purpose: Antimicrobial
Hand Sanitizer
FDA Label NDC 78313-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cangzhou Zhuo Wang Trade Co., Ltd for the product Hand Sanitizer (NDC 78313-101). 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, warnings, do not use, 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
Antimicrobial
Use
Hand sanitizer to help decrease bacteria on skin.
Recommended for repeated use.
Warnings
For external use only.
Flammable. Keep away from hire or flame.
Do Not Use
- on children less than 2 months of age
- on open skin wounds
Otc - Stop Use
Stop use and ask doctor if irritation or rash appears and lasts.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. Children must be superised in use of this product.
Directions
Put enough product on hands to cover all surfaces. Rub hands together, until hands feel dry.
Other Information
Do not store above 110℉(43℃).
May discolor certain fabrics or surfaces.
Inactive Ingredients
Glycerol, Sodium hyaluronate, Trolamine, Carbomer, Water.
Package Label - Principal Display Panel
300 (300)
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