Otc - Active Ingredient
Active Ingredient
Benzalkonium Chloride
Hand Sanitizer
FDA Label NDC 29500-9088
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Personal Care Products for the product Hand Sanitizer (NDC 29500-9088). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, warnings, dosage & administration, inactive ingredient, indications & usage, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Antimicrobial
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
Warnings
Warnings:
For external use only.
When using this product: Avoid contact with eyes. In case of eye contact, flush with plenty of water. Avoid contact with broken skin.
Stop use and ask a doctor if irritation develops.
Dosage & Administration
Directions:
Wet hands thoroughly with product and rub into skin until dry.
For children under 6, use only under adult supervision.
Not recommended for infants.
Inactive Ingredient
Inactive Ingredients
Water(Aqua), Benzalkoinum chloride, cetrimonium chloride, disodium cocoamphodicetate, fragrance, glycerin, citric acid, dimethicone, tetrasodium EDTA
Indications & Usage
Use: To reduce bacteria on the skin.
Package Label.Principal Display Panel
Label (Foaminghandsanitizer)
Personal Care
Alcohol Free
Foaming Hand Sanitizer
Superior protection
Kills 99.9% of germs*
Clean Fresh Scent
7 fl oz (207 ml)
* Please review the disclaimer below.
