SANITAXE ANTIBACTERIAL- benzalkonium chloride gel 
American Consumer Products Corp

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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Sanitaxe Hand Soap

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

Sanitaxe Hand Soap

SANITAXE ANTIBACTERIAL 
benzalkonium chloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72197-009
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.26 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
WATER (UNII: 059QF0KO0R)  
SODIUM COCOAMPHOACETATE (UNII: W7Q5E87674)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
PEG-250 DISTEARATE (UNII: FHP1R1SR0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72197-009-27800 mL in 1 BOX; Type 0: Not a Combination Product06/30/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/30/2020
Labeler - American Consumer Products Corp (081101181)

Revised: 6/2020
Document Id: a8c6ef84-b073-72ee-e053-2995a90aa111
Set id: a8c6ef84-b072-72ee-e053-2995a90aa111
Version: 1
Effective Time: 20200623
 
American Consumer Products Corp