GOJO ANTIMICROBIAL FOAM HANDWASH WITH PCMX- chloroxylenol liquid 
GOJO Industries, 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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GOJO Antimicrobial Foam Handwash with PCMX

Active ingredient

Chloroxylenol 0.5%

Purpose

Antimicrobial

Use

Warnings

For external use only

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts

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

Directions

Inactive ingredients

Water (Aqua), Alcohol, Lauric Acid, Ethanolamine, Dipropylene Glycol, Lactic Acid, Poloxamer 124, Isopropyl Alcohol, Sodium Metabisulfite, Sodium Sulfite, Tetrasodium EDTA, Sodium Sulfate, Fragrance (Parfum), Methylparaben, Propylparaben, Green 3 (CI 42053), Red 33 (CI 17200)

Product Label

GOJO ANTIMICROBIAL FOAM HANDWASH WITH PCMX 
chloroxylenol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-521
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.005 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
LAURIC ACID (UNII: 1160N9NU9U)  
MONOETHANOLAMINE (UNII: 5KV86114PT)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
LACTIC ACID (UNII: 33X04XA5AT)  
POLOXAMER 124 (UNII: 1S66E28KXA)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
SODIUM SULFITE (UNII: VTK01UQK3G)  
EDETATE SODIUM (UNII: MP1J8420LU)  
SODIUM SULFATE (UNII: 0YPR65R21J)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:21749-521-53535 mL in 1 BOTTLE; Type 0: Not a Combination Product07/30/2014
2NDC:21749-521-97700 mL in 1 BOTTLE; Type 0: Not a Combination Product07/30/2014
3NDC:21749-521-891200 mL in 1 BOTTLE; Type 0: Not a Combination Product07/30/2014
4NDC:21749-521-901250 mL in 1 BOTTLE; Type 0: Not a Combination Product07/30/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/30/2014
Labeler - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIBusiness Operations
GOJO Industries, Inc.036424534manufacture(21749-521)
Establishment
NameAddressID/FEIBusiness Operations
GOJO Industries, Inc.088312414label(21749-521) , pack(21749-521)

Revised: 10/2017
Document Id: d746a3b9-4ac9-43e6-935f-deff6267bdfa
Set id: 1f531296-f826-4354-919a-ed356d70e4ba
Version: 2
Effective Time: 20171016
 
GOJO Industries, Inc.