Label: ACNE AND BLEMISH CONTROL MASK- sulfer cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 19, 2023

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

  • Active ingredient

    Sulfur 5%

  • Purpose

    Acne Treatment

  • Uses:

    For the treatment of acne

  • Warnings:

    For external use only

    When using this product

    skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irriation occurs, only use one topical acne medication at a time. Avoid contact with eyes. Apply only to areas with acne. Do not use on broken skin or large areas of the skin.

    Stop an dask a doctor

    if rash or irritation develops and lasts.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions:

    Clean the skin thoroguhly before applying this product. Cover the entire affected area with a thin layer. Leave on for 10-15 minutes. Rinse skin with warm water. Use 1-2 times a week. Can be applied on pimple as a spot treatment.

  • Inactive ingredients:

    WATER, KAOLIN, GLYCERIN, CAPRYLIC/CAPRIC TRIGLYCERIDE, NIACINAMIDE, GUM ARABIC, CETYL ALCOHOL, BENTONITE, CETEARYL ALCOHOL, CETEARETH-20, BUTYROSPERMUM PARKII (SHEA) BUTTER, SALICYCLIC ACID, HYDROLYZED ARDENIA FLORIDA EXTRACT, MENTHA PIPERITA (PEPPERMINT) OIL, EUCALYPTUS GLOBULUS LEAF OIL, SALIX NIGRA (WILLOW) BARK EXTRACT, TANACETUM ANNUUM, TOCOPHERYL ACETATE, ALOE BARBADENSIS LEAF JUICE, ALPHA-ARBUTIN, KOJIC ACID, AZELAIC ACID, RETINYL PALMITATE, TOCOPHEROL OIL, VACCINIUM MACOCARPON (CRANBERRY) FRUIT EXTRACT, XANTHAN GUM, MALTODEXTRIN, SODIUM PCA, CAMELLIA SINENSIS (GREEN TEA) LEAF EXTRACT, GLUTATHIONE, TARTARIC ACID, CITRIC ACID, PHENOXYETHANOL, ETHYLHEXAYLGLYCERIN.

  • PRINCIPAL DISPLAY PANEL

    AcneMask

  • INGREDIENTS AND APPEARANCE
    ACNE AND BLEMISH CONTROL MASK 
    sulfer cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70809-1906
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    GARDENIA JASMINOIDES WHOLE (UNII: 0PK353KHF0)  
    ACACIA (UNII: 5C5403N26O)  
    BENTONITE (UNII: A3N5ZCN45C)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CRANBERRY JUICE (UNII: Y74M3X3345)  
    SODIUM PIDOLATE (UNII: 1V74VH163T)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    AZELAIC ACID (UNII: F2VW3D43YT)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    TARTARIC ACID (UNII: W4888I119H)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    GLUTATHIONE (UNII: GAN16C9B8O)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    MENTHA PIPERITA (UNII: 79M2M2UDA9)  
    SALIX NIGRA BARK (UNII: QU52J3A5B3)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TANSY OIL (UNII: 43J2812KE1)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    KAOLIN (UNII: 24H4NWX5CO)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALPHA-ARBUTIN (UNII: 72VUP07IT5)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    WATER (UNII: 059QF0KO0R)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    KOJIC ACID (UNII: 6K23F1TT52)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70809-1906-11 in 1 BOX04/28/2020
    173.93 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00604/28/2020
    Labeler - USRX LLC (115270633)
    Establishment
    NameAddressID/FEIBusiness Operations
    Packaging On Demand, Inc.610511326manufacture(70809-1906)