Label: NATURIUM SULFUR SPOT TREATMENT 8%- sulfur liquid

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

Drug Label Information

Updated November 14, 2023

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

  • Drug Facts

  • Active Ingredient

    Sulfur 8.0%

  • Purpose

    Acne treatment

  • Uses

    • Helps clear up acne blemishes and helps prevent new acne blemishes from forming.
  • 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 irritation occurs, only use one topical acne medication at a time.
    • apply only to areas with acne
    • Avoid eye area. In case of eye contact, flush gently and thoroughly with water.

    Do not use on

    • broken skin
    • large areas of the skin

    Keep out of reach of children.


  • Directions

    Shake Well

    • clean the skin thoroughly before applying this product
    • cover the entire affected area with a thin layer one to three times daily
    • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
    • if bothersome dryness or peeling occurs, reduce application to once a day or every other day.
    • if going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use and ask a doctor.
  • Other Information

    Sensitivity Test for a New User. Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated above.Store in controlled temperatures (4-20°C/39-68°F). Keep in a dark and dry place. Keep container tightly closed.

  • Inactive Ingredients

    Aqua (Water), Kaolin, Aluminum Starch Octenylsuccinate, Propanediol, Glyceryl Stearate, Niacinamide, Acacia Senegal Gum, Cetearyl Alcohol, Glycerin, Ganoderma Lucidum Extract, Acetyl Glucosamine, Aloe Barbadensis Leaf Juice, Tranexamic Acid, Citric Acid, Xanthan Gum, Phenoxyethanol, Tocopheryl Acetate, Ethylhexylglycerin, 1,2-Hexanediol, Caprylyl Glycol, Potassium Sorbate, Sodium Benzoate, Tocopherol.

  • Product Packaging

    1

  • INGREDIENTS AND APPEARANCE
    NATURIUM SULFUR SPOT TREATMENT 8% 
    sulfur liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76354-120
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR80 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    KAOLIN (UNII: 24H4NWX5CO)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    ACACIA (UNII: 5C5403N26O)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GANODERMA LUCIDUM WHOLE (UNII: J5P04QW0CF)  
    N-ACETYLGLUCOSAMINE (UNII: V956696549)  
    TRANEXAMIC ACID (UNII: 6T84R30KC1)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76354-120-011 in 1 CARTON06/17/2022
    115 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00606/17/2022
    Labeler - e.l.f. Cosmetics, Inc (093902816)