FOAMING HAND- benzalkonium chloride soap

Foaming Hand by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredient

Benzalkonium chloride 0.13%

Purpose

Antibacterial

Use

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 thoroughly with water.

Stop use and ask a doctor if

• irritation or 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

Adverse event

DISTRIBUTED BY:

UPLIFT BRANDS, LLC

ST. LOUIS, MO 63114

1-866 MY GERMX

Principal display panel

germ-X ®

PRO

ANTIBACTERIAL

FOAMING

HAND SOAP

1000 ML (1.05 QT) 33.8 FL OZ

INGREDIENTS AND APPEARANCE

FOAMING HAND 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83986-224
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
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)
GLYCERIN (UNII: PDC6A3C0OX)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
EDETATE SODIUM (UNII: MP1J8420LU)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83986-224-08	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/11/2024
2	NDC: 83986-224-45	1150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/11/2024
3	NDC: 83986-224-86	1000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/11/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/11/2024

Labeler - UpLift Brands, LLC (119091527)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(83986-224)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(83986-224)