SANITAXE ANTIBACTERIAL- benzalkonium chloride gel

Sanitaxe Antibacterial by

Drug Labeling and Warnings

Sanitaxe Antibacterial by is a Otc medication manufactured, distributed, or labeled by American Consumer Products Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Active Ingredient

Benzalkonium Chloride .26%

Purpose

Purpose

Antiseptic

Uses

Uses ● Helps reduce bacteria on the skin that could cause disease. Recommended for repeated use.

Warnings

Warnings – For external use only. Do not ingest or swallow.

Flammable. Keep away from fire or flame.

Do not apply around eyes. Do not use in ears & mouth.

When using this product

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

Stop use and ask a doctor

Stop use and ask a doctor if redness or irritation develops and persists for more than 72 hours.

Keep out of reach of children

Keep out of reach of children. Do not use on children less than 2 months of age.

Supervise use in children under 6 years of age to prevent accidental swallowing.

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

Directions

Directions ● pump as needed on your palms and thoroughly spread on both hands

● rub into skin until dry.

Other information

Other information ● store at room 20° C (68° to 77° F) ● may discolor fabrics.

Inactive ingredients

Inactive ingredients: Water (Aqua), Cocamidopropyl Betane, PEG-6000 Disterate, Sodium Cocoamphoacetate, Fragrance, Citric Acid, Methylisothiazolinone, Iodopropynyl Butylcarbamate

Sanitaxe Hand Soap

INGREDIENTS AND APPEARANCE

SANITAXE ANTIBACTERIAL 
benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72197-009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.26 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
PEG-250 DISTEARATE (UNII: FHP1R1SR0X)
WATER (UNII: 059QF0KO0R)
SODIUM COCOAMPHOACETATE (UNII: W7Q5E87674)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72197-009-27	800 mL in 1 BOX; Type 0: Not a Combination Product	06/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/30/2020

Labeler - American Consumer Products Corp (081101181)