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Omnicide Antimicrobial

Medically reviewed on April 15, 2018

Dosage form: gel
Ingredients: BENZALKONIUM CHLORIDE 0.13g in 100g
Labeler: SteriWeb Medical, LLC
NDC Code: 69085-466

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.

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

OMNICIDE ANTIMICROBIAL 
benzalkonium chloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69085-466
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE0.13 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER 
POLIHEXANIDE 
PETROLATUM 
Packaging
#Item CodePackage Description
1NDC:69085-466-0245 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/02/201404/30/2021
Labeler - SteriWeb Medical, LLC (079409860)

 
SteriWeb Medical, LLC

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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