Active Ingredient
Benzalkonium Chloride 0.1%
Decon7 Antiseptic Foaming Hand Sanitizer Liquid
FDA Label NDC 78245-201
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Decon7 Systems, Llc for the product Decon7 Antiseptic Foaming Hand Sanitizer (NDC 78245-201). 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, purpose, uses, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Uses
- For hand sanitizing to decrease bacteria on the skin
- Recommended for repeated use
Warnings
For external use only
Otc - When Using
When using this product avoid contact with eyes. In case of eye contact, flush eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develop or last 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
- Apply small amount of foam into palm of hand
- Rub hands together briskly covering surface of hands until dry
Inactive Ingredients
Water, cocamidopropyl PG-dimonium chloride phosphate, dihydroxyethyl cocamine oxide,acetamidoethoxyethanol, citric acid
Package Label.Principal Display Panel
Decon7 Antiseptic Foaming Hand Sanitizer
Manufactured in the USA for: D7™ DECON SEVEN
110 North Freeport Parkway, Suite 120, Coppell, TX 75019
844-727-FOAM / [email protected]
1.7 fl oz (50 mL)
24/7 Emergency Response,
Contact Chemtrec 800-424-9300
* Please review the disclaimer below.
