SureKill Hand Sanitizer by Preserve Inc / Preserve International SUREKILL HAND SANITIZER

SureKill Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

SUREKILL HAND SANITIZER- hand sanitizer liquid 
Preserve Inc

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SUREKILL HAND SANITIZER

DRUG FACTS
Active ingredients

Ethyl Alcohol 62%

PURPOSE

Antimicrobial

USES

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

WARNINGS

Flammalbe.  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 1-2 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 Perfluoroalkylethyl Phosphate, Glycerin

SUREKILL

Hand Sanitizer

• Kills 99.9% of harmful bacteria on contact.
• Quick Drying Foam
• Apply following persticide application

​Manufactured by: Preserve International ®

a wholly-owned subsidiary of Neogen ®

944 Nandino Blvd.

Lexington, KY  40511 USA

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

SUREKILL HAND SANITIZER 
hand sanitizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60648-8600
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
2-(PERFLUOROHEXYL)ETHANOL (UNII: G2R5YO5N3V)
PEG-10 ACRYLATE/PERFLUOROHEXYLETHYL ACRYLATE COPOLYMER (UNII: D76Z87928N)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60648-8600-2	16 in 1 PACKAGE, COMBINATION	07/25/2023	12/16/2024
1	NDC: 60648-8600-1	0.2 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
2	NDC: 60648-8600-4	4 in 1 PACKAGE, COMBINATION	07/25/2023	12/16/2024
2	NDC: 60648-8600-3	3.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	07/25/2023	12/16/2024

Labeler - Preserve Inc (808154199)

Registrant - Preserve International (117315289)

Establishment
Name	Address	ID/FEI	Business Operations
Preserve Inc		808154199	api manufacture(60648-8600) , manufacture(60648-8600)

Revised: 12/2024

Document Id: 29687328-e5c8-23cf-e063-6394a90a65fc

34390-5

Set id: 015614dc-e7e3-9275-e063-6294a90a1f1c

Version: 2

Effective Time: 20241216

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