ADVANCED HAND SANITIZER- ethyl alcohol gel 
UpLift Brands LLC

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Germ-X Advanced Hand Sanitizer with Aloe
439.001/439AB-AC rev1

Active ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

Warnings

For external 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, Aloe barbadensis leaf juice, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, carbomer or acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4, blue 1, yellow 5

Disclaimer

DSP-TN-21091 DSP-MO-20087 DSP-MO-28 SDS-MO-20068

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

FORMULA MADE IN USA 

EMPLOYY-OWNED

Advrse Reaction

Dist. by: Vi-Jon, LLC

8515 Page Ave.

St. Louis, MO 63114

Principal display panel

germ-x ®

SINCE 1997

ADVANCED

70% ALCOHOL HAND SANITIZER WITH ALOE

Kills more than 99.99% of Germs*

with added moisturizers

33.8 FL OZ (1L) 1.05 QT

image description

ADVANCED HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83986-439
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
SULISOBENZONE (UNII: 1W6L629B4K)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83986-439-1659 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product02/23/2024
2NDC:83986-439-34236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product02/23/2024
3NDC:83986-439-861000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/23/2024
4NDC:83986-439-32355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/23/2024
5NDC:83986-439-50709 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/23/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)02/23/2024
Labeler - UpLift Brands LLC (119091527)
Registrant - Consumer Product Partners, LLC (119091520)
Establishment
NameAddressID/FEIBusiness Operations
Consumer Product Partners, LLC119091520manufacture(83986-439)
Establishment
NameAddressID/FEIBusiness Operations
Consumer Product Partners, LLC119091514manufacture(83986-439)

Revised: 2/2024
Document Id: 120f2e4e-0148-f88a-e063-6294a90a2183
Set id: f6608379-051f-4151-bcf7-ecd87070f439
Version: 1
Effective Time: 20240223
 
UpLift Brands LLC