HAND SANITIZER- alcohol gel

Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredient

Ethyl alcohol 65%

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.
do not inhale or ingest avoid contact with broken skin

Stop use and ask a doctor if

skin irritation develops

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

wet hands thoroughly with product and allow to dry without wiping
for children under 6, use only under adult supervision
not recommended for infamts

Other information

do not store above 105⁰F  may discolor some fabrics
harmful to wood finishes and plastics

Inactive ingredients

aloe barbadensis leaf juice, benzophenone-4, blue 1, carbomer, fragrance, glycerin, isopropyl myristate, propylene glycol,
tocopheryl acetate, water, yellow 5

SPL UNCLASSIFIED SECTION

Effective at eliminating over 99.99% of many common harmful germs and bacteria in as little as 15 seconds.
SDS-MO-15036, SDA-WI-2059, SDA-WI-2486, DSP-MO-28, DSP-MO-34

Visit us at: Rexall.com
or call 1-866-4-REXALL
DISTRIBUTED BY DOLGENCORP, LLC
100 MISSION ROAD
GOODLETTSVILLE, TN 37072

principal display panel

Rexall
Hand Sanitizer
Moisturizing with Vitamin E and Aloe
Kills 99.99% of Harmful Germs
15 FL OZ (446 mL)

203.000/203AB

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55910-203
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	.65 mL  in 100 L

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SULISOBENZONE (UNII: 1W6L629B4K)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55910-203-49	.446 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/24/2000

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/24/2000

Labeler - Dolgencorp, LLC (068331990)

Registrant - Vi-Jon (088520668)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		088520668	manufacture(55910-203)