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PURELL Healthcare HEALTHY SP 0.5pct PCMX Antimicrobial Foam

Medically reviewed on Jul 14, 2017

Dosage form: liquid
Ingredients: CHLOROXYLENOL 0.005mg in 1mL
Labeler: GOJO Industries, Inc.
NDC Code: 21749-522

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.

PURELL Healthcare HEALTHY SOAP 0.5% PCMX Antimicrobial Foam

Active ingredient

Chloroxylenol 0.5%

Purpose

Antimicrobial

Use
  • Handwash to help reduce bacteria on the skin
  • Recommended for repeated use

Warnings

For external use only

Wwhen 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
  • Wet hands
  • Apply a small amount of product and work into a lather
  • Rinse well and dry hands completely

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

PURELL HEALTHCARE HEALTHY SP 0.5PCT PCMX ANTIMICROBIAL FOAM 
chloroxylenol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-522
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (CHLOROXYLENOL) CHLOROXYLENOL0.005 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water 
ALCOHOL 
LAURIC ACID 
MONOETHANOLAMINE 
DIPROPYLENE GLYCOL 
LACTIC ACID 
POLOXAMER 124 
ISOPROPYL ALCOHOL 
SODIUM METABISULFITE 
SODIUM SULFITE 
EDETATE SODIUM 
SODIUM SULFATE 
METHYLPARABEN 
PROPYLPARABEN 
Packaging
#Item CodePackage Description
1NDC:21749-522-53535 mL in 1 PACKAGE
2NDC:21749-522-891200 mL in 1 PACKAGE
3NDC:21749-522-901250 mL in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/14/2017
Labeler - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIOperations
GOJO Industries, Inc.036424534manufacture(21749-522)
Establishment
NameAddressID/FEIOperations
GOJO Industries, Inc.088312414label(21749-522), pack(21749-522)

 
GOJO Industries, Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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