Active Ingredient(S)
Ethyl Alcohol 68% w/w. Purpose: Antiseptic
Hand Sanitizer
FDA Label NDC 75613-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Lanzi Cosmetic Technology Co., Ltd for the product Hand Sanitizer (NDC 75613-101). 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 - 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
Antiseptic
Use
For hand sanitizing to reduce bacteria on the skin.
Warnings
Flammable.
Keep away from fire or flame.
For external use only.
Do not inhale or ingest.
Do Not Use
Do not inhale or ingest.
Otc - When Using
When using this product Keep out of eyes.
In case of contact, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash appears or lasts.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Squeeze out enough product in your palm to cover hands and rub hands together briskly until dry.
Other Information
Store below 110℉ (43℃).
Inactive Ingredients
Ethyl Alcohol, Glycerin, Propylene Glycol, Triethanolamine, Carbomer, Fragrance, Disodium EDTA, Tocopheryl Acetate, Deionized Water.
Package Label - Principal Display Panel
Label (Label)
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