Ethyl Alcohol by Vi-Jon, LLC ETHYL ALCOHOL gel

Ethyl Alcohol by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 65%

Purpose

Antiseptic

Use

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

Warnings

For external use only-hands

Flammable.  Keep away from heat and 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

• skin irritation 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 105⁰ F
• may discolor some fabrics
• harmful to wood finishes and plastics

Inactive ingredients

benzophenone-4, carbomer, fragrance, glycerin, isopropyl myristate, propylene glycol, tocopheryl acetate, water

Rear Label Text

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

**Not manufactured or distributed by Johnson and Johnson, the owner and distributor of Purell Hand Sanitizer

Made in USA with US and foreign components

Distributed by Vi-Jon, 8515 page Ave.  St. Louis, MO 63114

principal display panel

Waterless Hand Sanitizer

Original

Kills 99.99% of germs*

Compare to Purell**

8 FL OZ (236 mL)

951.001/951AA-AB

INGREDIENTS AND APPEARANCE

ETHYL ALCOHOL 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11344-951
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	578 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SULISOBENZONE (UNII: 1W6L629B4K)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
glycerin (UNII: PDC6A3C0OX)
isopropyl myristate (UNII: 0RE8K4LNJS)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11344-951-16	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/08/2014
2	NDC: 11344-951-29	200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/08/2014
3	NDC: 11344-951-34	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/08/2014
4	NDC: 11344-951-38	296 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/08/2014
5	NDC: 11344-951-49	443 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/08/2014
6	NDC: 11344-951-45	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/08/2014
7	NDC: 11344-951-86	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/08/2014
8	NDC: 11344-951-88	2000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/08/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/08/2014

Labeler - Vi-Jon, Inc. (150931459)

Registrant - Vi-Jon, Inc. (088520668)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon, Inc.		088520668	manufacture(11344-951)