ANTIACTERIAL HAND SANITIZER- alcohol gel

Antiacterial Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 65%

Purpose

Antiseptic

Use

to decrease bacteria on the skin that could cause disease
recommended for reported 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, flus 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  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

Not manufactured or distributed by GOJO Industries, owner of the registered trademark Purell

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

Dist by Target Corp
Mpls, MIN55403

principal display panel

Hand Sanitizer Gel with aloe
Compare to Purell
kills 99.99% of germs without water
Hygiene handshake
up + up
8 FL OZ (236.5 mL)

203.000/203AB

INGREDIENTS AND APPEARANCE

ANTIACTERIAL HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-203
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: 11673-203-16	.059 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/07/2011
2	NDC: 11673-203-34	.236 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/07/2011
3	NDC: 11673-203-45	.946 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/07/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/07/2011

Labeler - Target Corp (006961700)

Registrant - Vi-Jon (088520668)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		088520668	manufacture(11673-203)