Kelley's Hand Sanitizer Gel 65%

Alcohol by

Drug Labeling and Warnings

Alcohol by is a Otc medication manufactured, distributed, or labeled by K2 Distribution Company LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ALCOHOL- alcohol gel 
K2 Distribution Company LP

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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Kelley's Hand Sanitizer Gel 65%

Drug Facts

Active ingredient

Active ingredient Ethyl Alcohol 65% v/v

Purpose

Purpose Antimicrobial

Use

Use Hand sanitizer to help reduce bacteria on the skin

Warnings

Warnings

• Flammable. Keep away from fire and flame
• For external use only

When using thiss product

When using thiss product avoid use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if

Stop use and ask a doctor if irritation or rash occurs.

Keep out of reach of children

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

Directions

Directions Apply product generously in palm using enough to cover hands. Rub hands together until dry. Children under 6 years of age should be supervised when using this product.

Other information

• Protect the product in this container from excessive heat and direct sun. Store below 110°F (43°C).
• May discolor some fabrics or surfaces.

Inactive ingredients

Water, Hydroxyethylcellulose, Glycerin, Menthol, Cocoyl Argininamide, Safflower Acids, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Coconut Acids, Eucalyptus Globulus Leaf Oil, Caprylyl Glycol, Fragrance, 1,2-Hexanediol, Disodium EDTA-Copper.

Questions

Customer Service 888-458-1038

Kelley's Hand Sanitizer Gel

KILLS HARMFUL BACTERIA AND GERMS

Distributed by: K2 Distribution

128 fl oz (3785.4 ml)

triclosan, Sulfate & Paraben-Free

NOT FOR RESALE

ALCOHOL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78039-051
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
MENTHOL (UNII: L7T10EIP3A)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
SAFFLOWER ACID (UNII: Y788KS82OV)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
COCONUT ACID (UNII: 40U37V505D)
GLYCERIN (UNII: PDC6A3C0OX)
EUCALYPTUS OIL (UNII: 2R04ONI662)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78039-051-01	3785.4 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020	05/31/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/01/2020	05/31/2021

Labeler - K2 Distribution Company LP (117528256)

Revised: 11/2020

Document Id: b47e2fe3-921c-161e-e053-2995a90ae4be

34390-5

Set id: a71d0011-1751-60d4-e053-2a95a90ad083

Version: 2

Effective Time: 20201119