SUREKILL HAND SANITIZER GEL- 62% ethyl alcohol gel

SureKill Hand Sanitizer Gel by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 62% v/v

Purpose

Antimicrobial

Uses

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

Warnings

Flammable. Keep away from fire or flame.

For external use only.

WHEN USING

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

STOP USE

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

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

Directions

• Squeeze product into palm of hand.
• 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, Glycerin, Aloe Vera

Principal Display Panel

SureKill® HAND SANITIZER GEL

• Kills 99.9% of harmful bacteria on contact
• Quick Drying Gel

Net Contents: 8 oz. (236mL)

Item No. 490911/8SK 

NEOGEN®

Manufactured For:

Neogen® Corporation

944 Nandino Blvd. Lexington, KY 40511 USA

800-621-8829 (USA/Canada) or 859-254-1221 L6946-0420

INGREDIENTS AND APPEARANCE

SUREKILL HAND SANITIZER GEL 
62% ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59051-4909
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59051-4909-7	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/24/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/24/2020

Labeler - Neogen Corporation (042125879)