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Kelleys Advanced Hand Sanitizer

Dosage form: gel
Ingredients: ALCOHOL 65mL in 100mL
Labeler: K2 Distribution Company LP
NDC code: 78039-062

Medically reviewed by Drugs.com. Last updated on Jul 22, 2024.

Kelley's Advanced Hand Sanitizer Gel

Drug Facts

Active ingredient

Ethyl Alcohol 65%

Purpose

Antiseptic

Uses

Hand sanitizer to help reduce bacteria on the skin that can cause disease.

Directions

Apply liberally to front and back of hands. Allow to dry. Recommended for repeated use.

Warnings

For external use only: hands

Flammable, keep away from fire or flame.

When using this product

When using this product avoid contact with the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor

Stop use and ask a doctor if irritation or redness appears and lasts.

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.

Do not use

Do not use: in children less than 2 months of age and on open wounds. Do not inhale or ingest. Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

Store between 0°C (32°F) - 41°C (105°F)

Inactive ingredients

Acrylates copolymer, aloe barbadensis (aloe) extract, fragrance, glycerin, sodium hydroxide, water

Questions

Customer Service 888-458-1038

Kelley's Adanced Hand Sanitizer Gel

KILLS 99.99% OF ILLNESS CAUSING GERMS

WITH MOISTURIZING ALOE

Distributed by: K2 Distribution

128 fl oz

Triclosan, sulfate & paraben-free

NOT FOR RESALE

KELLEYS ADVANCED HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78039-062
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL65 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN 
WATER 
ALOE VERA LEAF 
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) 
SODIUM HYDROXIDE 
Packaging
#Item CodePackage Description
1NDC:78039-062-013785.4 mL in 1 BOTTLE
2NDC:78039-062-023785.4 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/31/2020
Labeler - K2 Distribution Company LP (117528256)

Revised: 07/2020
 
K2 Distribution Company LP

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.