HANDI-KLEEN ANTIBACTERIAL FOAMING HAND WASH- chloroxylenol liquid 
Diamond Chemical Co. Inc.

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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Handi-Kleen Antibacterial Foaming Hand Wash

Drug Facts

Active Ingredient

Cloroxylenol 0.3% w/w

Purpose

Antiseptic

Uses

Warnings

For external use only.

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

Stop use and ask a doctor if irritation or redness develop or if condition persists for more than 72 hours.

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

Directions

Inactive Ingredients Water, Sodium Laureth Sulfate, Cocamide DEA, DMDM Hydantoin, Ethyl Alcohol, Phenoxyethanol, Isopropyl Alcohol, Fragrance, Citric Acid, FD&C Red 4

Handi-Kleen™

Antibacterial Foaming Hand Wash

1000 ML (33.8 FL.OZ.) CARTRIDGE

DISTRIBUTED BY:

STARCO CHEMICAL

A Division of Diamond Chemical Co., Inc.

Union Ave & Dubois Street East Rutherford, NJ 07073 • (201) 935-4300

72177-180

HANDI-KLEEN ANTIBACTERIAL  FOAMING HAND WASH
chloroxylenol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72177-180
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
COCAMIDOPROPYL DIMETHYLAMINE (UNII: L36BM7DG2T)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
ALCOHOL (UNII: 3K9958V90M)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72177-180-101000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product02/03/202107/26/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E02/03/202107/26/2024
Labeler - Diamond Chemical Co. Inc. (001381482)

Revised: 9/2022
Document Id: e99b21f7-5d92-95da-e053-2995a90a944a
Set id: ba6fcc25-4a32-57f6-e053-2995a90ae913
Version: 3
Effective Time: 20220926
 
Diamond Chemical Co. Inc.