SureKill Hand Sanitizer by 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 International. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SUREKILL HAND SANITIZER- hand sanitizer liquid 
Preserve International

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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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: 60648-8100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	338.82 L  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: 60648-8100-2	16 in 1 PACKAGE, COMBINATION	03/03/2020	07/25/2023
1	NDC: 60648-8100-1	0.20 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
2	NDC: 60648-8100-4	4 in 1 PACKAGE, COMBINATION	03/03/2020	07/25/2023
2	NDC: 60648-8100-3	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 not final	part333E	03/03/2020	07/25/2023

Labeler - Preserve International (808154199)

Registrant - Preserve International (808154199)

Establishment
Name	Address	ID/FEI	Business Operations
Preserve International		808154199	manufacture(60648-8100) , api manufacture(60648-8100)

Revised: 7/2023

Document Id: ae9e407b-f80f-4f43-8597-75f8a606e76e

34390-5

Set id: 79661405-2841-4dec-ab9b-8395a751a1ee

Version: 3

Effective Time: 20230725