Active Ingredient(S)
Ethyl Alcohol 75.0%Antimicrobia
Hand Sanitizer
FDA Label NDC 77060-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Beta Industry And Trade Co., Ltd. for the product Hand Sanitizer (NDC 77060-101). 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, 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
Antimicrobial
Use
Uses help reduce bacteria on the skin.
Do Not Use
- in children less than 2 months of age
- on open skin wounds
Otc - When Using
When using this product avoid contact with face, eyes, and broken skin, In case of eye contact, flush with plenty of water and seek medical advice
Otc - Stop Use
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children, If swallowed, get medical help or contact a Poison Control Center.
Directions
Directions: wet hands thoroughly with product and rubinto skin until dry. Children under 6 years of age should be supervised by an adult when using
Other Information
- Store between 15-30C (59-86F)
- Avoid freezing and excessive heat above 40C (104F)
Inactive Ingredients
water(aqua), triethanolamine, carbomer, aloealoe barbadensis(aloe vera)leaf juice,fragrance, glycerin, propylene glycol,tocopherol Acetate(Vitamin E)
Package Label - Principal Display Panel
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