Hand Sanitizer by Vi- Jon, LLC / Vi-Jon, LLC Germ-X 899

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- ethyl alcohol spray 
Consumer Product Partners, LLC

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Germ-X 899

Active ingredient

Ethyl alcohol 62%

purpose

Antiseptic

Use

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

Warnings

For external use only

Flammable.  Keep away from fire or flame

When using this product

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

Stop use and ask a doctor if

• irritation or 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

• spray 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 105°F
• may discolor some fabrics
• harmful to wood finishes and plastics

Inactive ingredients

water, glycerin, Aloe barbadensis leaf juice, fragrance, limonene

Questions

1-866-MYGERMX

1-866-694-3769

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

Distributed By: Vi-Jon, LLC

8515 Page AVe., St. Louis, MO 63114

www.germx.com

principal display panel

germ-X

since 1997

KILLS 99.99% OF GERMS

HAND SANITIZER SPRAY

CITRUS SCENT

KILLS GERMS IN 15 SECONDS

FORMULA MADE IN USA

EMPLOYEE OWNED

2 FL OZ (59 mL)

HAND SANITIZER 
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11344-899
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.62 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
LIMONENE OXIDE, (+)- (UNII: 278IM94GXB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11344-899-20	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/06/2016	04/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(c)	06/06/2016	04/01/2024

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(11344-899)

Revised: 4/2024

Document Id: 151dbee6-d28e-d957-e063-6394a90a7f63

34390-5

Set id: 1c6311fa-67a8-4e9e-b69b-6dc8b32dc393

Version: 6

Effective Time: 20240402