ADVANCED HAND SANITIZER- alcohol gel
CVS Pharmacy, Inc

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.

----------

Drug Facts

active ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Uses

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 develops

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

water, aloe, barbadensis leaf juice, glyceryl, caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4, blue 1, yellow 5

Claims

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

SDS-MO-15036, SDA-WI-2486, DSP-MO-28, DSP-MO-34

Adverse Reactions

Distributed by:

CVS Pharmacy, Inc

One CVS Drive

Woonsockot, RI 02805

www.cvs.com 1-800-shop-CVS

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

Principal display panel

CVS

Pharmacy

advanced

formula

hand

sanitizer

with aloe

Kills more than 99.99% of germs

Leaves hands feeling soft

Moisturizing formula

with aloe + vitamin E

32 FL OZ (946 mL)

image description

ADVANCED HAND SANITIZER
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG LABEL	Item Code (Source)	NDC:59779-070
Route of Administration	TOPICAL	DEA Schedule

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (ALCOHOL)	ALCOHOL	700 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER
ALOE VERA LEAF
GLYCERYL CAPRYLATE/CAPRATE
GLYCERIN
ISOPROPYL MYRISTATE
.ALPHA.-TOCOPHEROL ACETATE
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
SULISOBENZONE
FD&C BLUE NO. 1
FD&C YELLOW NO. 5

#	Item Code	Package Description
Packaging
1	NDC:59779-070-16	59 mL in 1 BOTTLE, DISPENSING
2	NDC:59779-070-34	236 mL in 1 BOTTLE, PUMP
3	NDC:59779-070-45	946 mL in 1 BOTTLE, PUMP
4	NDC:59779-070-26	118 mL in 1 BOTTLE, PUMP
5	NDC:59779-070-49	443 mL in 1 BOTTLE, PUMP

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	10/18/2013

Labeler - CVS Pharmacy, Inc (062312574)

Registrant - Vi-Jon (790752542)

Name	Address	ID/FEI	Business Operations
Establishment
Vi-Jon		088520668	manufacture(59779-070)

Revised: 2/2014

Document Id: 1a302965-3ab7-48d5-b0d8-fc9492377f08

Set id: 2adb16b7-c43f-49a0-9a56-fece3d730089

Version: 1

Effective Time: 20140221

CVS Pharmacy, Inc