COMPANION HAND SANITIZER- hand sanitizer liquid

Companion Hand Sanitizer by

Drug Labeling and Warnings

Companion Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Neogen Corporation, Preserve International. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTSActive ingredients

Ethyl Alcohol 62%

PURPOSE

Antimicrobial

USES

• For hand sanitizing to decrease disease causing dermal bacteria
• Recommend for repeated use.

WARNINGS

Flammable.  Keep away from fire or flame.

For External use only.

When using this product avoid contact with eyes.  In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if 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

Place 2 pumps of product into your palm.  Rub hands together briskly until dry.  Children under 6 years of age should be supervised when using this product.

OTHER INFORMATION

Store below 110°F (43°C). May discolor certain fabrics or surfaces.

INACTIVE INGREDIENTS

Water, DEA C8-18, Glycerin

PRINCIPAL DISPLAY PANEL

COMPANION

Hand Sanitizer

• Kills 99.9% of harmful bacteria on contact.
• Foaming action.

NET CONTENTS: 7 oz.

Item No.: 490909/16

Manufactured For: Neogen Corporation

944 Nandino Blvd.

Lexington, KY  40511 USA

800-477-8201 (USA/Canada) or 859-254-1221  L4849-1216

INGREDIENTS AND APPEARANCE

COMPANION HAND SANITIZER 
hand sanitizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59051-7100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	338.82 g  in 1 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PEG-10 ACRYLATE/PERFLUOROHEXYLETHYL ACRYLATE COPOLYMER (UNII: D76Z87928N)
2-(PERFLUOROHEXYL)ETHANOL (UNII: G2R5YO5N3V)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59051-7100-2	16 in 1 PACKAGE, COMBINATION	06/05/2017
1	NDC: 59051-7100-1	0.20 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/05/2017

Labeler - Neogen Corporation (042125879)

Registrant - Preserve International (808154199)

Establishment
Name	Address	ID/FEI	Business Operations
Preserve International		808154199	manufacture(59051-7100) , api manufacture(59051-7100)