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PCMX with Emollient (Aplicare, Inc.)

Available Formats

Dosage Form Package Information Links
SOLUTION 189 kg in 1 DRUM (52380-9957-9) Label Information
SOLUTION .09 kg in 1 BOTTLE (52380-9957-3) Label Information
SOLUTION .12 kg in 1 BOTTLE (52380-9957-4) Label Information

Complete PCMX with Emollient Information

  • ACTIVE INGREDIENT

    3.3% w/w Chloroxylenol


  • INDICATIONS & USAGE

    Uses

    For cleansing hands and forearms prior to surgery or patient care


  • PURPOSE

    Antiseptic


  • WARNINGS

    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.


  • DOSAGE & ADMINISTRATION

    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

  • INACTIVE INGREDIENT

    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

    Questions?

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


  • PRINCIPAL DISPLAY PANEL

    Scrub Care 3.3% Chloroxylenol

    Emmollient CLeansing Solution

    Label


  • INGREDIENTS AND APPEARANCE
    PCMX WITH EMOLLIENT 
    chloroxylenol solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:52380-9957
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 3.3 mg  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    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 Code Package Description Marketing Start Date Marketing End Date
    1 NDC:52380-9957-3 946 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/20/2018
    2 NDC:52380-9957-4 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/20/2018
    3 NDC:52380-9957-9 208198 mL in 1 DRUM; Type 0: Not a Combination Product 02/20/2018
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 05/01/2004
    Labeler - Aplicare Products, LLC. (081054904)
    Establishment
    Name Address ID/FEI Business Operations
    Aplicare Products, LLC. 081068252 manufacture(52380-9957)