Apothecary Home Antibacterial Men Hand Soap 21.5 fl.oz

Apothecary Home Men by

Drug Labeling and Warnings

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

Drug Details [pdf]

APOTHECARY HOME MEN- 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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Apothecary Home Antibacterial Men Hand Soap 21.5 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

APOTHECARY HOME MEN 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73746-038
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
EDETATE SODIUM (UNII: MP1J8420LU)
GLYCERIN (UNII: PDC6A3C0OX)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73746-038-01	636 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/07/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/07/2020	10/05/2022

Labeler - HOME & BODY COMPANY (081290720)

Registrant - HOME & BODY COMPANY (081290720)

Establishment
Name	Address	ID/FEI	Business Operations
HOME & BODY COMPANY		081290720	manufacture(73746-038)

Revised: 10/2022

Document Id: ea61affc-9f10-7983-e053-2a95a90ae58c

34390-5

Set id: a9e2eae1-2421-9b30-e053-2995a90a543b

Version: 5

Effective Time: 20221006