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Little Me Sanitizer
FDA Label NDC 76860-006
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 Liweir Cosmetic Technology Ltd. for the product Little Me Sanitizer (NDC 76860-006). 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 other, active ingredient(s), purpose, use, warnings, 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
Active Ingredient(S)
Benzalkonium Chloride 0.13%
Purpose
Antibacterial Agent
Use
for hand-washing to decrease bacteria on the skin, only when water is not available
Warnings
For external use only
Otc - When Using
When using the product do not get into eyes. If contact occurs, rinse thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation occurs or rash develops and continues for more than 72 hours.
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
adults and children 2 years and over
- apply to hands
- allow skin to dry without wiping
children under 2 years
ask a doctor before use
Inactive Ingredients
Water, Glycerin, PEG-40 Hydrogenated Castor Oil, Chlorhexidine Digluconate, Benzethonium Chloride, Fragrance (Parfum).
Package Label.Principal Display Panel
76860-006-01 (76860 006 01)
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