Dye Free Germ-X Hand Sanitizer with Aloe 996.000/996AA

Advanced Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

ADVANCED HAND SANITIZER- ethyl alcohol gel 
Consumer Product Partners, LLC

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Dye Free Germ-X Hand Sanitizer with Aloe 996.000/996AA

Active ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

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

Warnings

For external 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 thoroughly with water.
• avoid contact with broken skin
• do not inhale or ingest

Stop use and ask a doctor if

• irritation and redness develop
• conditon 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 105⁰ F
• may discolor some fabrics
• harmful to wood finishes and plastics

Inactive ingredients

water, Aloe barbadensis leaf juice, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, carbomer, fragrance

disclaimer

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

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

Distributed By Vi-Jon, LLC.

8515 Page Ave., St. Louis, MO 63114

FORMULA MADE IN

USA

EMPLOYEE OWNED

Pat. 9,161,982

principal display panel

GERM-X

SINCE 1997

ADVANCED

moisturizing

hand sanitizer

with Aloe & Vitamin E

Kills more than 99.99% of germs in 15 seconds*

70% ETHYL ALCOHOL

FORMULA MADE IN USA

EMPLOYEE OWNED

12 FL OZ (354 ML)

ADVANCED HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11344-996
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	700 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERYL MONOCAPRYLOCAPRATE (UNII: G7515SW10N)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11344-996-16	59 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	12/02/2020	03/09/2024
2	NDC: 11344-996-34	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	12/02/2020
3	NDC: 11344-996-49	443 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	12/02/2020	03/09/2024
4	NDC: 11344-996-45	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/02/2020	03/09/2024
5	NDC: 11344-996-88	2000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/02/2020	03/09/2024
6	NDC: 11344-996-48	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/02/2020	03/09/2024
7	NDC: 11344-996-32	355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/02/2020	03/09/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/02/2020	03/09/2024

Labeler - Consumer Product Partners, LLC (119091520)

Registrant - Vi-Jon, LLC (088520668)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon, LLC		088520668	manufacture(11344-996)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon, LLC		790752542	manufacture(11344-996)

Revised: 3/2024

Document Id: 13468e2d-5774-85a9-e063-6294a90a2e6a

34390-5

Set id: e057c32c-8ca1-4d9d-acfc-480537fd5044

Version: 12

Effective Time: 20240309