HAND SANITIZER- alcohol gel

Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredient

Active ingredient

Ethyl alcohol 70%

purpose

Purpose

Antiseptic

Uses

Uses

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

Warnings

Warnings

For external use only-hands

Flammable

Flammable. Keep away from heat and flame

When using

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

Stop use and ask a doctor if skin irritation develops

Keep out of reach of children

Keep out of reach of children. If swallowed get nedical help or contact a Poison Control Center right away

Directions

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

Other information

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

Inactive ingredients

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

Claims

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

Disclaimer

This product is no manufactured or distributed by GOJO Industries, Inc., distributor of Purell refreshing Gel Advanced Hand Sanitizer

Adverse Reactions Section

DISTRIBUTED BY: CARDINAL HEALTH, DUBLIN, OHIO 43017

www.myleader.com

Principal Display Panel

NDC: 37205-733-34

LEADER

More

Effective

Formula

Compare to Purell

Advanced

Hand

Sanitizer

Kills more than 99.99% of germs

8 FL OZ (236 mL)

SPL UNCLASSIFIED SECTION

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37205-733
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: 37205-733-34	236 mL in 1 BOTTLE, PUMP

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/09/2012

Labeler - Cardinal Health (097537435)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		088520668	manufacture(37205-733)