Active Ingredient(S)
ETHYL ALCOHOL：70%
Instant Hand Sanitizer Liquid
FDA Label NDC 75541-016
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 Meiteli Cosmetics Co., Ltd for the product Instant Hand Sanitizer (NDC 75541-016). 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 - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Use
Uses hand sanitizer to help reduce bacteria on the skin.
Warnings
Warnings For external use only.
Do Not Use
Children under two years old, please do not use
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 redness develops.
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 rub
into skin until dry. ■Children under 6 years of age should be
supervised by an adult when using.
Other Information
Flammable. Keep away from heat and flame.
Inactive Ingredients
Inactive ingredients aqua(water), acrylates/c10-30
alkyl acrylate crosspolymer, aminomethyl propanol, aloe
barbadensis leaf juice, denatonium benzoate, fragrance,
glycerine, propylene glycol, tocopheryl acetate
Package Label - Principal Display Panel
Label (Label)
Undefined (Label1)
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