HAND SANITIZER- ethyl alcohol gel

Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredient

Ethyl alcohol 62%

Purpose

Antiseptic

Uses

• to decrese bacteria on the skin that could cause disease
• 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

• irritation or redness develops
• 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, Aloe barbadensis leaf juice, tocopheryl acetate, carbomer, isopropyl myristate, isopropyl alcohol, propylene glycol, fragrance, blue 1, yellow 5

Questions?

Call 1-800-789-1331

back of label

*Effective at eliminating 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

Distributed by: Quill.com, 100 Schelter Road, Lincolnshire, IL 60069

472.000/472AA

principal display panel

Moisturizing Hand Sanitizer with Aloe and Vitamin E

Kills 99.99% of germs*

Quill.com

10 FL OZ (295 mL)

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49514-472
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	545 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49514-472-16	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/16/2016
2	NDC: 49514-472-38	295 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/16/2016
3	NDC: 49514-472-88	2000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/16/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/16/2016

Labeler - Staples the Office Superstore, LLC (151064821)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		088520668	manufacture(49514-472)