ALCOHOL- alcohol liquid 
Consumer Product Partners, LLC

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Germ-X Hand Sanitizer
826.000/826AA rev 1

Active ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

  • for handwashing to decrease bacteria on the skin that could cause disease
  • recommended for repeated use

Warnings

For exterenal use only: hands

Flammable, keep away from fire or flame.

When using this product

  • keep out of eyes. In case of contact with eyes, flush thoroghly with water.
  • avoid contact with broken skin
  • do not inhale or ingest

Stop use and ask a doctor if

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

Other information

  • do not store above 105⁰F
  • may discolor some fabrics
  • harmful to wood finishes and plastics

Inactive ingredients

water, carbomer, fragrance, glycerin, isopropyl myristate, Aloe barbadensis leaf juice, tocopheryl acetate, blue 1, yellow 5

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

Distributed By: Vi-Jon, LLC

www.germx.com

Principal Display Panel

germ-X

ORIGINAL

MOISTURIZING HAND SANITIZER WITH ALOE

Kills 99.99% of Germs*

with vitamin E

2 FL OZ (59 mL)

image description

ALCOHOL 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11344-826
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)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11344-826-32355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/19/201704/29/2024
2NDC:11344-826-1659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/07/2019
3NDC:11344-826-481005 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/19/201704/29/2024
4NDC:11344-826-511770 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/19/201704/29/2024
5NDC:11344-826-2189 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/30/201904/29/2024
6NDC:11344-826-34236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/30/201904/29/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)07/19/201704/29/2024
Labeler - Consumer Product Partners, LLC (119091520)
Registrant - Consumer Product Partners, LLC (119091520)
Establishment
NameAddressID/FEIBusiness Operations
Consumer Product Partners, LLC119091520manufacture(11344-826)
Establishment
NameAddressID/FEIBusiness Operations
Consumer Product Partners, LLC119091514manufacture(11344-826)

Revised: 4/2024
Document Id: 17420029-919d-9b3d-e063-6294a90a5fae
Set id: 8d59f7c6-656a-46a8-8da1-f4844351b5d3
Version: 41
Effective Time: 20240429
 
Consumer Product Partners, LLC