Label: CUTAR- coal tar lotion

  • NDC Code(s): 11086-105-01, 11086-105-02
  • Packager: Summers Laboratories Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 9, 2023

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    7.5% L.C.D. (EQUIVALENT TO 1.5% COAL TAR)

  • PURPOSE

    PURPOSE

    PSORIASIS, SEBORREIC DERMATITIS TREATMENT

  • INDICATIONS & USAGE

    USE

    • CONTROLS ITCHING, FLAKING AND REDNESS DUE TO PSORIASIS AND SEBORRHEIC DERMATITIS
  • WARNINGS

    WARNINGS

    FOR EXTERNAL USE ONLY

  • ASK DOCTOR

    ASK A DOCTOR BEFORE USE IF YOU HAVE

    • CONDITION THAT COVERS A LARGE AREA OF THE BODY
    • CONDITION IN OR AROUND THE RECTUM, GENITAL AREA OR GROIN
  • WHEN USING

    WHEN USING THIS PRODUCT

    • AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER
    • USE CAUTION IN EXPOSING SKIN TO SUNLIGHT AFTER APPLYING THIS PRODUCT. IT MAY INCREASE YOUR TENDENCY TO SUNBURN FOR UP TO 24 HOURS AFTER APPLICATION
  • DO NOT USE

    DO NOT USE

    • FOR PROLONGED PERIODS WITHOUT CONSULTING A DOCTOR
    • WITH OTHER FORMS OF PSORIASIS THERAPY UNLESS DIRECTED TO DO SO BY A DOCTOR
  • STOP USE

    STOP USE AND ASK A DOCTOR IF

    • CONDITION WORSENS OR DOES NOT IMPROVE AFTER REGULAR USE AS DIRECTED
    • EXCESSIVE IRRITATION OCCURS
  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

    • IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY
    • TO PREVENT STAINING DO NOT USE IN PLASTIC OR FIBERGLASS TUBS, SINKS OR BASINS. CUTAR MAY STAIN LIGHT COLORED FABRICS
  • DOSAGE & ADMINISTRATION

    DIRECTIONS

    • APPLY TO AFFECTED AREAS ONE TO FOUR TIMES DAILY OR AS DIRECTED BY A DOCTOR
    • AS A MEDICATED LOTION: GENTLY RUB A SMALL AMOUNT ONTO AFFECTED AREAS. BLOT OFF EXCESS WITH A TISSUE TO HELP PREVENT STAINING OF CLOTHING OR LINENS
    • IN THE BATH: POUR A LIBERAL QUANTITY (2 TO 4 OZ.) INTO THE TUB, MAKING SURE CUTAR IS WELL MIXED. SOAK FOR 10 TO 20 MINUTES, OR AS DIRECTED BY YOUR DOCTOR. AFTER TREATMENT, PAT SKIN DRY.
    • GUARD AGAINST SLIPPING.
    • AS A HAND OR FOOT SOAK: ADD 1 TO 2 OZ. TO A SINK OR BASIN. MIX WELL AND SOAK FOR 5 TO 10 MINUTES OR AS DIRECTED BY YOUR DOCTOR.
  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS

    WATER, MINERAL OIL, ISOPROPYL MYRISTATE, POLYSORBATE 80, SORBITAN SESQUIOLEATE, LANOLIN ALCOHOLS EXTRACT, METHYL AND PROPYL PARABENS, FRAGRANCE, XANTHAN GUM, CARBOMER

  • PRINCIPAL DISPLAY PANEL

    CUT6 label 0417

  • INGREDIENTS AND APPEARANCE
    CUTAR 
    coal tar lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11086-105
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    COAL TAR (UNII: R533ESO2EC) (COAL TAR - UNII:R533ESO2EC) COAL TAR1.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
    LANOLIN ALCOHOLS (UNII: 884C3FA9HE)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11086-105-01180 mL in 1 BOTTLE; Type 0: Not a Combination Product10/29/2013
    2NDC:11086-105-023785 mL in 1 JUG; Type 0: Not a Combination Product10/29/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03210/29/2013
    Labeler - Summers Laboratories Inc (002382612)