Skip to Content

← See all Ethyl Alcohol brands

Ethyl Alcohol by Vi-Jon, Inc.

Medically reviewed on August 15, 2017

Dosage form: gel
Ingredients: ALCOHOL 578mg in 1mL
Labeler: Vi-Jon, Inc.
NDC Code: 11344-951

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Swan Waterless Hand Sanitizer

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

ETHYL ALCOHOL 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11344-951
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL578 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SULISOBENZONE 
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) 
glycerin 
isopropyl myristate 
PROPYLENE GLYCOL 
.ALPHA.-TOCOPHEROL ACETATE 
WATER 
Packaging
#Item CodePackage Description
1NDC:11344-951-1659 mL in 1 BOTTLE, PLASTIC
2NDC:11344-951-29200 mL in 1 BOTTLE, PLASTIC
3NDC:11344-951-34236 mL in 1 BOTTLE, PLASTIC
4NDC:11344-951-38296 mL in 1 BOTTLE, PLASTIC
5NDC:11344-951-49443 mL in 1 BOTTLE, PLASTIC
6NDC:11344-951-45946 mL in 1 BOTTLE, PLASTIC
7NDC:11344-951-861000 mL in 1 BOTTLE, PLASTIC
8NDC:11344-951-882000 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A09/08/2014
Labeler - Vi-Jon, Inc. (150931459)
Registrant - Vi-Jon, Inc. (088520668)
Establishment
NameAddressID/FEIOperations
Vi-Jon, Inc.088520668manufacture(11344-951)

 
Vi-Jon, Inc.

← See all Ethyl Alcohol brands

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Hide