OMNICIDE ANTIMICROBIAL- benzalkonium chloride gel 
SteriWeb Medical, 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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STERIWEB RX (as PLD) - OMNICIDE FIRST AID ANTIMICROBIAL GEL (69085-466-03) - DELIST

Active Ingredient

Benzalkonium Chloride   0.13% w/w

Purpose

First Aid Antiseptic

Uses

First aid to help treat, protect and prevent skin infection associated with

  • minor cuts
  • scrapes
  • burns

Warnings

For external use only

Ask a doctor before use if you have

  • deep or puncture wounds
  • animal bites
  • serious burns

When using this product

  • Do not use in or near the eyes
  • Do not use if you have a history of allergy to any of the ingredients

Stop and ask a doctor if

  • condition worsens
  • symptoms persist for more than 7 days, or clear up and occur again within a few days.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away

Directions

  • adults and children 2 years and older: clean the affected area; apply a small amount on the area 1-3 times daily; may be covered with a sterile bandage (let dry first)
  • children under 2 years: ask a doctor

Other information

Avoid excessive heat.

Inactive Ingredients

USP Petrolatum, Water, Polihexanide (PHBM)

Questions?

1-360-448-7881

or www.steriwebrx.com

Principal Display Panel

STERIWEB MEDICAL

Omnicide Antimicrobial Gel

First Aid Antimicrobial Gel

Hospital and Professional Use Only

Omnicide is a registered trademark of Steriweb Medical

omnicide

OMNICIDE ANTIMICROBIAL 
benzalkonium chloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69085-466
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
POLIHEXANIDE (UNII: 322U039GMF)  
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69085-466-035 g in 1 TUBE; Type 0: Not a Combination Product07/02/201412/31/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/02/201412/31/2016
Labeler - SteriWeb Medical, LLC (079409860)

Revised: 9/2023
 
SteriWeb Medical, LLC