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PCMX with Emollient

Medically reviewed on November 10, 2016

Dosage form: solution
Ingredients: CHLOROXYLENOL 3.3mg in 100mL
Labeler: Aplicare, Inc.
NDC Code: 52380-9957

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.

Drug Facts

3.3% w/w Chloroxylenol

Uses

For cleansing hands and forearms prior to surgery or patient care

Antiseptic

For external use only

Do not use in the eyes

Stop use and ask a doctor if

  • skin shows symptoms of irritation, sensitivity, redness, pain or swelling
  • discontinue use if irritation and redness develop. If condition persists more than 72 hours consult a doctor.

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

Directions

  • Clean under nails with nail pick. Nails should be maintained with a 1 mm free edge
  • Wet hands and forearms
  • Apply 5 ml or palmful to hands and forearms
  • Scrub thoroughly for 3 minutes with a wet brush
  • Pay particular attention to the nails, cuticles and interdigital spaces
  • Rinse thoroughly with running water
  • Repeat

Other information
  • Store at room temperature
  • Avoid excessive heat above 40 deg C (104 deg F)
  • Protect from freezing
  • Latex Free

Citric Acid, PEG-120 Methyl Glucose Dioleate, Phenoxyethanol, Propylene Glycol, Purified Water, Sodium C12-15 Pareth-15 Sulfonate, Sodium Hydroxide, Sodium Lauroyl Sarcosinate, Sodium Laryl Sulfate, Soy Acid, Styrene/VP Copolymer

Questions?

Call: 1-800-523-0502 (Mon. - Fri. 8 AM-5 PM CST)

Scrub Care 3.3% Chloroxylenol

Emmollient CLeansing Solution

PCMX WITH EMOLLIENT 
chloroxylenol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52380-9957
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (CHLOROXYLENOL) CHLOROXYLENOL3.3 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM C12-15 PARETH-15 SULFONATE 
SOY ACID 
WATER 
SODIUM LAUROYL SARCOSINATE 
PROPYLENE GLYCOL 
PEG-120 METHYL GLUCOSE DIOLEATE 
SODIUM LAURYL SULFATE 
PHENOXYETHANOL 
ANHYDROUS CITRIC ACID 
SODIUM HYDROXIDE 
Packaging
#Item CodePackage Description
1NDC:52380-9957-3946 mL in 1 BOTTLE
2NDC:52380-9957-4118 mL in 1 BOTTLE
3NDC:52380-9957-9208198 mL in 1 DRUM
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/01/2004
Labeler - Aplicare, Inc. (107255002)
Establishment
NameAddressID/FEIOperations
Aplicare058377631manufacture(52380-9957)

 
Aplicare, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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