Garrison + Home 22 fl.oz Antibacterial Hand Soap

Garrison Home by

Drug Labeling and Warnings

Garrison Home by is a Otc medication manufactured, distributed, or labeled by HOME & BODY COMPANY. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

GARRISON HOME- 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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Garrison + Home 22 fl.oz Antibacterial Hand Soap

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

21.5 purplerefil purplerefill black label

GARRISON HOME 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 73746-036
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)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 73746-036-01636 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/17/2020
2NDC: 73746-036-021893 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/20/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/13/202008/12/2023
Labeler - HOME & BODY COMPANY (081290720)
Registrant - HOME & BODY COMPANY (081290720)
Establishment
NameAddressID/FEIBusiness Operations
HOME & BODY COMPANY081290720manufacture(73746-036)

Revised: 10/2022
Document Id: ea619f8f-f6a4-0fab-e053-2a95a90a1e01
Set id: a7fd734c-8f7c-f51c-e053-2995a90a5b47
Version: 8
Effective Time: 20221006