Otc - Active Ingredient
Active ingredient
Benzalkonium Chloride 0.1%
Puracy Natural Foaming Hand Sanitizer
FDA Label NDC 72905-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Puracy Llc for the product Puracy Natural Foaming Hand Sanitizer (NDC 72905-001). 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, indications & usage, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Antimicrobial
Indications & Usage
Uses
for hand sanitizing to decrease bacteria on the skin
recommended for repeated use
Warnings
Warnings
For external use only
Otc - When Using
When using this product avoid contact with eyes.
In case of eye contact, flush eyes with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develops, or if condition persists 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.
Dosage & Administration
Directions
pump a small amount of foam into palm of hand
rub thoroughly over all surfaces of both hands
rub hands together briskly until dry
Inactive Ingredient
Inactive ingredients
Water, cetrimonium chloride, laurtrimonium chloride, dihydroxyethyl cocamine oxide, glycereth-17 cocoate, citric acid
Package Label.Principal Display Panel
puracy
NATURAL FOAMING
HAND SANITIZER
alcohol-free kills 99.9% of germs
FRAGRANCE FREE
Austin Texas 8.5 fl.oz. (251 mL)
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