Label: LIQUIMAT ACNE TREATMENT AND COVER-UP- sulfur liquid

  • NDC Code(s): 11086-028-01
  • Packager: Summers Laboratories Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 27, 2024

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  • ACTIVE INGREDIENT

    ACTIVE INGREDIENT

    SULFUR 4%

  • PURPOSE

    PURPOSE

    ACNE TREATMENT LOTION

  • INDICATIONS & USAGE

    USE

    DRIES UP ACNE PIMPLES, HELPS PREVENT NEW PIMPLES

  • WARNINGS

    WARNINGS

    • FOR EXTERNAL USE ONLY
  • DO NOT USE

    DO NOT USE

    • ON BROKEN SKIN
    • ON LARGE AREAS OF THE BODY
  • WHEN USING

    WHEN USING THIS PRODUCT

    • APPLY TO AFFECTED AREAS ONLY
    • DO NOT GET INTO EYES
    • USING OTHER TOPICAL ACNE DRUGS AT THE SAME TIME OR RIGHT AFTER USE OF THIS PRODUCT MAY INCREASE DRYNESS OR IRRITATION OF THE SKIN. IF THIS OCCURS, ONLY ONE DRUG SHOULD BE USED UNLESS DIRECTED BY A DOCTOR
  • STOP USE

    STOP USE AND ASK A DOCTOR IF

    • TOO MUCH IRRITATION DEVELOPS OR INCREASES

    KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

  • DOSAGE & ADMINISTRATION

    DIRECTIONS

    • CLEAN SKIN THOROUGHLY BEFORE USING
    • COVER THE ENTIRE AFFECTED AREA WITH A THIN LAYER 1 TO 3 TIMES DAILY
    • BECAUSE TOO MUCH DRYING OF THE SKIN MAY OCCUR, START WITH 1 APPLICATION DAILY, THEN INCREASE TO 2 TO 3 TIMES DAILY IF NEEDED OR AS DIRECTED BY A DOCTOR.
  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS

    WATER, SD-40 ALCOHOL 22-PERCENT, KAOLIN, ZINC OXIDE, GLYCERIN, TITANIUM DIOXIDE, TALC, CELLULOSE GUM, MAGNESIUM ALUMINUM SILICATE, CETYL ALCOHOL, POLOXAMER 182, FRAGRANCE, IRON OXIDES. COLOR MATCHER CONTAINS IRON OXIDES, PEG-8, PEG-8 LAURATE, SIMETHICONE.

  • PRINCIPAL DISPLAY PANEL

    Liquimat_Unit Carton

  • INGREDIENTS AND APPEARANCE
    LIQUIMAT  ACNE TREATMENT AND COVER-UP
    sulfur liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11086-028
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M) 22 mL  in 100 mL
    KAOLIN (UNII: 24H4NWX5CO)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    WATER (UNII: 059QF0KO0R)  
    TALC (UNII: 7SEV7J4R1U)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    POLOXAMER 182 (UNII: JX0HIX6OAG)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    PEG-8 LAURATE (UNII: 762O8IWA10)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11086-028-0144 mL in 1 BOTTLE; Type 0: Not a Combination Product10/30/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00610/30/2013
    Labeler - Summers Laboratories Inc (002382612)
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