HAND SANITIZER- alcohol gel

Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredient

Ethyl alcohol 63%

Purpose

Antiseptic

Use

• for handwashing to decrease bacteria on the skin
• 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
• 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 105⁰F
• may discolor some fabrics
• harmful to wood finishes and plastics

inactive ingredients

water, glycerin, tocopheryl acetate, acrylates/C10-30 alkyl acrylate crosspolymer, benzophenone-4, fragrance, blue 1, red 33

claims

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

 Made in the U.S.A with U.S. and foreign components

Adverse reaction 

Distributed by: CVS Pharmacy, Inc

One CVS Drive, Woonsocket, RI 02895

CVS.com 1-800-SHOP CVS

593.000/593AB

principal display panel

garden orchard scent

hand sanitizer

kills 99.99% of germs

fast & effective

moisturizing formula with vitamin E

leaves hands feeling soft

CVS/pharmacy

2 FL OZ (59 mL)

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59779-593
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	567 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
SULISOBENZONE (UNII: 1W6L629B4K)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59779-593-16	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/23/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/23/2015

Labeler - CVS Pharmacy, Inc (062312574)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		088520668	manufacture(59779-593)