Kelley's Hand Sanitizer Gel

Kelleys Advanced Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

KELLEYS ADVANCED HAND SANITIZER- 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

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

purified water, methylcellulose, glycerin

Questions

Customer Service 888-458-1038

Kelley's Hand Sanitizer Gel

KILLS HARMFUL BACTERIA AND GERMS

Distributed by: K2 Distribution

128 fl oz

Triclosan, sulfate & paraben-free

NOT FOR RESALE

LABEL

KELLEYS ADVANCED HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 78039-041
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL65 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
METHYLCELLULOSE, UNSPECIFIED (UNII: Z944H5SN0H)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 78039-041-013785.4 mL in 1 BOTTLE; Type 0: Not a Combination Product04/01/202004/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/01/202004/01/2022
Labeler - K2 Distribution Company LP (117528256)

Revised: 4/2020
Document Id: b451b2dd-b810-8d40-e053-2a95a90a3377
Set id: b451b825-8f50-303a-e053-2a95a90ad941
Version: 1
Effective Time: 20200401