PCMX WITH EMOLLIENT- chloroxylenol solution 
Aplicare Products, 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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PCMX with Emollient

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

Other information

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

Label

PCMX WITH EMOLLIENT 
chloroxylenol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52380-9957
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL3.3 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM C12-15 PARETH-15 SULFONATE (UNII: 353VA59XH8)  
SOY ACID (UNII: HBA528N3PW)  
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
WATER (UNII: 059QF0KO0R)  
SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52380-9957-3946 mL in 1 BOTTLE; Type 0: Not a Combination Product02/20/2018
2NDC:52380-9957-4118 mL in 1 BOTTLE; Type 0: Not a Combination Product02/20/2018
3NDC:52380-9957-9208198 mL in 1 DRUM; Type 0: Not a Combination Product02/20/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/01/2004
Labeler - Aplicare Products, LLC. (081054904)
Establishment
NameAddressID/FEIBusiness Operations
Aplicare Products, LLC.081068252manufacture(52380-9957)

Revised: 2/2018
Document Id: 65a8bec7-b3b1-1919-e053-2991aa0a6540
Set id: 9fc5ad9e-66cd-42e9-8bc8-43f44eee27a2
Version: 5
Effective Time: 20180220
 
Aplicare Products, LLC.