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

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Vi-Jon, LLC, Vi Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND SANITIZER- alcohol gel 
Consumer Product Partners, LLC

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

Active ingredient

Ethyl alcohol 62%

Purpose

Antiseptic

Uses

• 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 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

HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11344-652
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11344-652-16	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/06/2022	04/25/2024
2	NDC: 11344-652-34	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/06/2022	04/25/2024
3	NDC: 11344-652-04	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/06/2022	04/25/2024
4	NDC: 11344-652-45	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/06/2022	04/25/2024
5	NDC: 11344-652-86	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/06/2022	04/25/2024
6	NDC: 11344-652-48	1150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/06/2022	04/25/2024
7	NDC: 11344-652-68	2000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/06/2022	04/25/2024
8	NDC: 11344-652-08	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/06/2022	04/25/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M505G(a)(3)	12/06/2022	04/25/2024

Labeler - Consumer Product Partners, LLC (119091520)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(11344-652)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(11344-652)

Revised: 4/2024

Document Id: 16ef3797-7f33-62a1-e063-6294a90ae139

34390-5

Set id: a6240ce0-ea7b-406b-9eb7-09892f8fbf91

Version: 2

Effective Time: 20240425