ANTIBIOTIC FREE WOUND GEL- benzalkonium chloride gel 
ASO 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.

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Antibiotic Free Wound Gel

Active ingredient (in each gram)

Benzalkonium Chloride 0.13%

Purpose

first aid antiseptic

Uses

  • First aid to help prevent infection in minor cuts, scrapes and burns

Warnings

For external use only

Do not use

  • in the eyes
  • over large areas of the body
  • longer than a week unless directed by a doctor

Ask a doctor before use if you have

  • deep or puncture wounds
  • animal bites
  • serious burns

Stop use and ask a doctor if

the condition persists or gets worse

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

  • Clean the affected area
  • apply a small amount of this product on the area 1 to 3 times daily
  • may be covered with a sterile bandage
  • if bandaged, let dry first

Other information

  • Store at room temperature

Inactive ingredients

caprylyl glycol, chlorphenesin, edetate disodium, glycerin, hydroxyethyl cellulose, phenoxyethanol, polysorbate 20, purified water

Principal Display Panel

Antibiotic Free

Wound Gel

0.13% BENZALKONIUM CHLORIDE

First aid antiseptic

Antibacterial Gel

  • For treating minor cuts, scrapes, and burns
  • Water-based clear hydrogel
  • Helps reduce scarring
  • Helps prevent infection

NET WT 1 OZ (28 g)

labe wound gel

ANTIBIOTIC FREE WOUND GEL 
benzalkonium chloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51142-650
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51142-650-321 in 1 CARTON03/21/201711/12/2022
128 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/21/201711/12/2022
Labeler - ASO LLC (152793493)

Revised: 2/2021
 
ASO LLC