Kelley's Advanced 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 Advanced Hand Sanitizer Gel

Drug Facts

Active ingredient

Alcohol 65%

Purpose

Antiseptic

Uses

  • to help reduce bacteria on the skin that can cause disease
  • recommended for repeated use

Warnings

For external use only

Flammable, keep away from fire or flame.

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

Stop use and ask a doctor if irritation or redness appears and lasts more than 72 hours

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

Directions

  • apply liberally to hands to cover all surfaces
  • rub hands together until dry
  • supervise children under 6 years old
  • not recommended for infants

Other information

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

Inactive ingredients

Water, acrylates copolymer, glycerin, aloe barbadensis (aloe) extract, fragrance, sodium hydroxide

Questions? 888-458-1038

Kelley's Adanced Hand Sanitizer Gel

WITH MOISTURIZING ALOE

1 Gallon (3.78L)

Triclosan, sulfate & paraben-free

NOT FOR RESALE

Distributed by:

K2 Distribution Company LP

950 Loveridge Rd, Pittsburgh, CA 94565

label

KELLEYS ADVANCED HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 78039-062
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)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 78039-062-013785.4 mL in 1 BOTTLE; Type 0: Not a Combination Product07/31/202008/31/2021
2NDC: 78039-062-023785.4 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/31/202008/31/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/31/202008/31/2021
Labeler - K2 Distribution Company LP (117528256)

Revised: 1/2022
Document Id: d66a2ce7-46ed-2e63-e053-2a95a90abd46
Set id: abc4959e-0d4d-26bc-e053-2995a90af2d9
Version: 3
Effective Time: 20220125