OMNICIDE ANTIMICROBIAL- benzalkonium chloride gel

Omnicide Antimicrobial by

Drug Labeling and Warnings

Omnicide Antimicrobial by is a Otc medication manufactured, distributed, or labeled by SteriWeb Medical, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

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

INGREDIENTS AND APPEARANCE

OMNICIDE ANTIMICROBIAL 
benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69085-466
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
POLIHEXANIDE (UNII: 322U039GMF)
PETROLATUM (UNII: 4T6H12BN9U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69085-466-02	45 g in 1 TUBE; Type 0: Not a Combination Product	07/02/2014	04/30/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/02/2014	04/30/2021

Labeler - SteriWeb Medical, LLC (079409860)