GREENEX ANTIBACTERIAL- chloroxylenol liquid 
Cleanslate Group LLC

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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Greenex Foam Hand Soap

Drug Facts

Active Ingredient

Parachlorometaxylenol 0.3% w/w

Purpose

Antiseptic

Uses

  • Handwash to help reduce bacteria on the skin that potentially can cause disease.
  • Recommended for repeated use.

Warnings

  • For external use only.

  • Keep out of eyes, ears or mouth. 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

  • Wet hands with water and dispense sufficient amount of product into cupped palm of hand.
  • Wash both hands thoroughly for 15 seconds.
  • Rinse under running water and dry thoroughly.

Inactive Ingredients

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

GREENEX

2 Bergen Turnpike

Ridgefield Park, NJ 07660

MADE IN THE USA

GREENEX

ANTIBACTERIAL FOAM HAND SOAP

With 0.3% PCMX

1000 ml

Greenex Individual Label

GREENEX ANTIBACTERIAL 
chloroxylenol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80586-513
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)  
COCO DIETHANOLAMIDE (UNII: 92005F972D)  
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:80586-513-101000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product04/13/202106/14/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/13/202106/14/2023
Labeler - Cleanslate Group LLC (117657934)

Revised: 9/2022
Document Id: e99b3955-65fe-f942-e053-2995a90a6e14
Set id: bfdbacb4-1afd-6e91-e053-2a95a90a7ba0
Version: 3
Effective Time: 20220926
 
Cleanslate Group LLC