FOAMING HAND SANITIZER- benzalkonium chloride liquid 
UpLift Brands LLC

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Germ-X 118.001/118.401/118AE-AF
Foaming Hand Sanitizer

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

Stop use and ask a doctor if

Keep out of reach of children.

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

Directions

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.

Made in USA with US and foreign parts

Adverse reactions

Distributed By: Vi-Jon, Inc.

8515 Page Ave, St. Louis, MO 63114

Principal display panel

germ-X

alcohol free

foaming hand sanitizer

Kills 99.99% of Germs*

Fresh Scent

7.5 FL OZ (221 mL)

image description

FOAMING HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83986-118
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
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83986-118-96221 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/29/2024
2NDC:83986-118-44532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/29/2024
3NDC:83986-118-861000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/29/2024
4NDC:83986-118-451150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/29/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)02/29/2024
Labeler - UpLift Brands LLC (119091527)
Registrant - Consumer Product Partners, LLC (119091520)
Establishment
NameAddressID/FEIBusiness Operations
Consumer Product Partners, LLC119091520manufacture(83986-118)
Establishment
NameAddressID/FEIBusiness Operations
Consumer Product Partners, LLC119091514manufacture(83986-118)

Revised: 2/2024
Document Id: 128b0a32-e3e9-9b1f-e063-6294a90a8809
Set id: f8ca7e87-e5f1-4ef2-b389-02d318ccf78f
Version: 2
Effective Time: 20240229
 
UpLift Brands LLC