HAND SANITIZER- alcohol gel 
UpLift Brands, LLC

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Germ-X 652.000/652AA rev 1
Hand Sanitizer Original Scent

Active ingredient

Ethyl alcohol 62%

Purpose

Antiseptic

Uses

Warnings

For exterenal use only: hands

Flammable, keep away from fire or flame.

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

Other information

Inactive ingredients

water, carbomer or acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, glycerin, isopropyl myristate, tocopheryl acetate

Disclaimer and Claim

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

FORMULA MADE IN USA 

EMPLOYEE OWNED

Adverse Reaction

Distributed By Vi-Jon, LLC

St. Louis, MO 63114

www.germx.com

Principal panel display

NEW LOOK!

SAME FORMULA

germ-X®

SINCE 1997

ORINGINAL

MOISTURIZING HAND SANITIZER

Kills 99.99% of Germs*

with vitamin E

8 FL OZ 236 mL

image description

HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83986-652
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
TOCOPHEROL (UNII: R0ZB2556P8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83986-652-1659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/06/2022
2NDC:83986-652-34236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/06/2022
3NDC:83986-652-04750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/06/2022
4NDC:83986-652-45946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/06/2022
5NDC:83986-652-861000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/06/2022
6NDC:83986-652-481150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/06/2022
7NDC:83986-652-682000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/06/2022
8NDC:83986-652-083785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/06/2022
9NDC:83986-652-552082 mL in 1 DRUM; Type 0: Not a Combination Product12/06/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)12/06/2022
Labeler - UpLift Brands, LLC (119091527)
Registrant - Consumer Product Partners, LLC (119091520)
Establishment
NameAddressID/FEIBusiness Operations
Consumer Product Partners, LLC119091520manufacture(83986-652)
Establishment
NameAddressID/FEIBusiness Operations
Consumer Product Partners, LLC119091514manufacture(83986-652)

Revised: 4/2024
Document Id: 16ef0d25-7095-d4e9-e063-6394a90a0c72
Set id: 3d1d8284-7392-4cb4-a7e5-8892d09129b2
Version: 1
Effective Time: 20240425
 
UpLift Brands, LLC