HAND SANITIZER- ethyl alcohol gel

Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

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

Warnings

For external use only: hands

Flammable.  Keep away from fire 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

• 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 thoroghly 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, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4

Questions?

Call (507) 454-5374

SPL UNCLASSIFIED SECTION

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

Part #0622139

Distributed by Fastenal

Company and its Subsidiaries

Winona, MN 55987

2017 fastenal.com

Made in USA with US and Foreign Components 

Distributed Exclusively by Fastenal

770.000/770AA

principal display panel

Clean

Choice

ANTIBACTERIAL

HAND SANITIZER GEL

Fresh Citrus

Kills More Than 99.99% of Many Common Harmful Germs and Bacteria

& Moisturizers & Vitamin E

8 FL OZ (236 mL)

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72024-770
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
SULISOBENZONE (UNII: 1W6L629B4K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72024-770-26	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/03/2018
2	NDC: 72024-770-34	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/03/2018
3	NDC: 72024-770-32	335 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/03/2018
4	NDC: 72024-770-88	2000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/03/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/03/2018

Labeler - Fastenal (042653634)

Registrant - Vi-Jon, Inc. (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon, Inc.		088520668	manufacture(72024-770)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon, Inc.		150931459	manufacture(72024-770)