ACTIVE GUARD- benzalkonium chloride liquid 
HOME & BODY COMPANY

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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Active Guard Antibacterial Soap 32fl.oz & 24.5 fl.oz

Active ingredient

0.13% Benzalkonium Chloride

Purpose

Antibacterial

Use

Helps reduce bacterial on hands

Warning

For external use only.
When using this product do not use in or near the eyes.
In case of contact, rinse eyes throughly with water.

Keep out of reach of children

Keep out of reach of children, except under adult supervision. If swallowed, get medical help or
contact a Poison Control Center right away.

Directions

Dispense soap into dry hands, work into lather and scrub for at least 35 seconds. Then rinse off with water.

Inactive Ingredients

Water (Aqua), Lauramine Oxide, Cellulose Gum, Tetrasodium EDTA, Polysorbate 20, Fragrance, Glycerin, Cocamidopropyl Betaine

Product Label

24 front24 back32 front32 back16

ACTIVE GUARD 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73746-037
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
EDETATE SODIUM (UNII: MP1J8420LU)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73746-037-01946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/29/2020
2NDC:73746-037-02724 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/29/2020
3NDC:73746-037-03473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/29/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/29/202010/05/2022
Labeler - HOME & BODY COMPANY (081290720)
Registrant - HOME & BODY COMPANY (081290720)
Establishment
NameAddressID/FEIBusiness Operations
HOME & BODY COMPANY081290720manufacture(73746-037)

Revised: 10/2022
Document Id: ea615a84-145a-3f43-e053-2995a90adfaa
Set id: a940ea4c-b9cc-c08a-e053-2a95a90a21f0
Version: 4
Effective Time: 20221006
 
HOME & BODY COMPANY