MOISTURIZING HAND SANITIZER- ethyl alcohol lotion

Moisturizing Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

claims

germ-x

MOISTURIZING

FOAMING

HAND SANITIZER

Active ingredient

Ethyl alcohol 62%

purpose

antiseptic

Uses

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

Warnings

For external use only - hands 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

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

Inactive ingredients

water, PEG-12 dimethicone, meadowfoamamidopropyl betaine, glycerin, tocopheryl acetate, isopropyl myristate

Adverse Reactions Section

Distributed By: Vi-Jon, Inc.

8515 Page Ave

St. Louis, MO 63114

principal display panel

germ-X

everywhere

MOISTURIZING

FOAMING

HAND SANITIZER

1150 mL (39 FL OZ)

INGREDIENTS AND APPEARANCE

MOISTURIZING HAND SANITIZER 
ethyl alcohol lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11344-447
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	Alcohol	.62 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
PEG-8 DIMETHICONE (UNII: GIA7T764OD)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11344-447-27	1150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/03/2016
2	NDC: 11344-447-07	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/03/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/03/2016

Labeler - Vi-Jon, Inc (150931459)

Registrant - Vi-Jon, Inc (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon, Inc		088520668	manufacture(11344-447)