FOAMING HAND- benzalkonium chloride soap

Foaming Hand by

Drug Labeling and Warnings

Foaming Hand by is a Otc medication manufactured, distributed, or labeled by VERITIV OPERATING COMPANY, Consumer Product Partners, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium chloride 0.13 %

Purpose

Antibacterial

Uses

for handwashing to decrease bacteria on the skin

Warnings

For external use only: hands only

When using this product

• avoid contact with eyes. If contact occurs, rinse eyes with water.

Stop use and ask a doctor if

• irritation and redness develop
• condition persists for more than 72 hours

Keep out of reach of children.

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

Directions

• wet hands
• apply palmful to hands
• scrub thoroughly
• rinse thoroughly

Inactive ingredients

water, cocamidopropyl betaine, lauramidopropylamine oxide, lauramine oxide, myristamidopropylamine oxide, glycerin, citric acid, tetrasodium EDTA, sodium benzoate

Claim

Product is NSF registered for use as a hand sanitizer in and around fool processing areas.

Adverse Reaction

Distributed by: Vestis

1035 Alpharetta Street

Suite 2100

Roswell, GA 30075

Principal Display Panel

vestis ®

NSF

Nonfood Compounds Program Listed E2 157038

Antibacterial

E2 Sanitizing

Foaming Hand Soap

Fragrance Free

33.8 FL OZ (1.05 QT) 1 L

INGREDIENTS AND APPEARANCE

FOAMING HAND 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71897-224
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
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
WATER (UNII: 059QF0KO0R)
CITRIC ACID (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)
TETRASODIUM EDTA (UNII: MP1J8420LU)
SODIUM BENZOATE (UNII: OJ245FE5EU)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71897-224-86	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	08/01/2025

Labeler - VERITIV OPERATING COMPANY (006989982)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(71897-224)