HAND SANITIZER- ethyl alcohol spray

Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredient

Ethyl alcohol 63%

purpose

Antiseptic

Use

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

Warnings

For external use 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

Stop use and ask a doctor if

• irritation or 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

• spray 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 105°F
• may discolor some fabrics
• harmful to wood finishes and plastics

Inactive ingredients

water, glycerin, tocopheryl acetate, Aloe barbadensis leaf juice, fragrance

claims

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

Adverse reaction

Distributed by: CVS Pharmacy, Inc.

One CVS Drive, Woonsocket, RI 02895

2017 CVS/pharmacy

CVS.com 1-800-SHOP CVS

Made in the U.S.A.

with U.S. and foreign

components   V-20332

CVS Quality

Money Back Guarantee

784.000/784AA

principal dispaly panel

vanilla citrus scent

natural

hand

sanitizer

spray

kills 99.99% of germs

dye free & hypoallergenic

plant-based alcohol

with aloe & vitamin E

CVSpharmacy

2 FL OZ (59 mL)

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-784
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	Alcohol	.63 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-784-20	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	02/22/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/22/2017

Labeler - CVS Pharmacy, Inc (062312574)

Registrant - Vi-Jon, Inc (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon, Inc		150931459	manufacture(69842-784)