FOAMING HAND SANITIZER- benzalkonium chloride liquid

Foaming Hand Sanitizer by

Drug Labeling and Warnings

Foaming Hand Sanitizer 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

Antiseptic

Use

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 thoroughly with water.
• avoid contact with broken skin

Stop use and ask a doctor if

• if irritation and redness develops
• 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 thoroughly with product and allow to dry without wiping
• for children under 6, use only under adult supervision
• not recommended for infants

Inactive ingredients

cetrimonium chloride, diglycerin, disodium cocoamphodiacetate, fragrance, glycerin, hydrochloric acid, methoxy PEG/PPG-7/3 aminopropyl dimethicone, sodium benzoate, tetrasodium EDTA, water

Claims

*Effective at eliminating 99.99% of many common harmful germs and bacteria in as little as 15 seconds.

Adverse reactions

DISTRIBUTED BY: 

UPLIFT BRANDS, LLC

ST. LOUIS, MO 63114

1-866 MY GERMX or 1-866-694-3769

Principal display panel

germ-X ®

ALCOHOL FREE

FOAMING

HAND SANITIZER

Kills 99.99% of Germs*

*KILLS GERMS IN 15 SECONDS

Fresh Scent

7.5 FL OZ (221 mL)

INGREDIENTS AND APPEARANCE

FOAMING HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83986-118
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
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
DIGLYCERIN (UNII: 3YC120743U)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROCHLORIC ACID (UNII: QTT17582CB)
METHOXY PEG/PPG-7/3 AMINOPROPYL DIMETHICONE (UNII: 4M7P1JZ2V2)
SODIUM BENZOATE (UNII: OJ245FE5EU)
EDETATE SODIUM (UNII: MP1J8420LU)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83986-118-96	221 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/29/2024
2	NDC: 83986-118-44	532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/29/2024
3	NDC: 83986-118-86	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/29/2024
4	NDC: 83986-118-45	1150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/29/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	02/29/2024

Labeler - UpLift Brands LLC (119091527)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(83986-118)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(83986-118)