COMPANION HAND SANITIZER- hand sanitizer liquid 
Neogen Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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COMPANION HAND SANITIZER

DRUG FACTS
Active ingredients

Ethyl Alcohol 62%

PURPOSE

Antimicrobial

USES

WARNINGS

Flammale.  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

COMPANION

Hand Sanitizer

​Manufactured For:Neogen Corporation

944 Nandino Blvd.

Lexington, KY  40511 USA

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

Companion Hand Sanitizer

COMPANION HAND SANITIZER 
hand sanitizer liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59051-7100
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL338.82 g  in 1 L
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
PEG-10 ACRYLATE/PERFLUOROHEXYLETHYL ACRYLATE COPOLYMER (UNII: D76Z87928N)  
2-(PERFLUOROHEXYL)ETHANOL (UNII: G2R5YO5N3V)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59051-7100-216 in 1 PACKAGE, COMBINATION06/05/2017
1NDC:59051-7100-10.2 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
2NDC:59051-7100-33.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/05/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/05/2017
Labeler - Neogen Corporation (042125879)
Registrant - Preserve International (117315289)
Establishment
NameAddressID/FEIBusiness Operations
Preserve Inc.808154199manufacture(59051-7100) , api manufacture(59051-7100)

Revised: 7/2023
Document Id: 01414006-6cbc-16fa-e063-6394a90adeab
Set id: 8b962905-c76a-4dec-b0e0-b0eb6a60c063
Version: 16
Effective Time: 20230724
 
Neogen Corporation