Decon7 Antiseptic Foaming Hand Sanitizer

Decon7 Antiseptic Foaming Hand Sanitizer by

Drug Labeling and Warnings

Decon7 Antiseptic Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Decon7 Systems, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DECON7 ANTISEPTIC FOAMING HAND SANITIZER- benzalkonium chloride liquid 
Decon7 Systems, LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Decon7 Antiseptic Foaming Hand Sanitizer

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

Uses

  • For hand sanitizing to decrease bacteria on the skin
  • Recommended for repeated use

Warnings

For external use only

When using this product avoid contact with eyes. In case of eye contact, flush eyes thoroughly with water.

Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.

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, fragrance

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 / info@decon7.com

1.7 fl oz (50 mL)

24/7 Emergency Response,

Contact Chemtrec 800-424-9300

50 mL label

1000 mL label

DECON7 ANTISEPTIC FOAMING HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 78245-101
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
WATER (UNII: 059QF0KO0R)  
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
ACETAMIDOETHOXYETHANOL (UNII: LVX2APC4XR)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 78245-101-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product11/22/202103/28/2024
2NDC: 78245-101-03550 mL in 1 BOTTLE; Type 0: Not a Combination Product11/22/202103/28/2024
3NDC: 78245-101-053800 mL in 1 BOTTLE; Type 0: Not a Combination Product11/22/202103/28/2024
4NDC: 78245-101-041000 mL in 1 BAG; Type 0: Not a Combination Product11/22/202103/28/2024
5NDC: 78245-101-061041000 mL in 1 CONTAINER; Type 0: Not a Combination Product11/22/202103/28/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A11/22/202103/28/2024
Labeler - Decon7 Systems, LLC (079281162)

Revised: 10/2022
Document Id: eb665069-0d05-c524-e053-2a95a90aeab2
Set id: d344f694-0055-d2d1-e053-2995a90a8f82
Version: 2
Effective Time: 20221019
 
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.