Label: ROYCEDERM SULFUR SOAP.- sulfur soap soap

  • NDC Code(s): 82739-023-01
  • Packager: Shenzhen Situya Trading Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 1, 2024

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

  • Active Ingredient

    Sulfur 10%

  • Purpose

    Acne Treatment

  • Use

    for the treatment of acne.

  • Warnings

    For external use only.

  • Do not use

    Use caution when combining with other topical acne medications to prevent skin irritation and dryness.

  • When Using

    When using this product avoid contact with eyes.
    If contact occurs, rinse the eyes thoroughly with water.

  • Stop Use

    stop use and ask a doctor if condition worsens or does not improve after regular use as directed.

  • Ask Doctor

    Discontinue use and consult a doctor ifexcessive skin irritation occurs.

  • Keep Oot Of Reach Of Children

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    Create a rich lather with the mesh bag, gently apply to affected areas, leaving it on the skin for 3 to 5 minutes. Rinse thoroughly with water and pat dry with a clean towel. Incorporate into your routine 1 to 3 times a day, or as directed by a doctor, for optimal results.

  • Other information

    ■ Store at room temperature and keep away from direct sunlight.

  • Inactive ingredients

    Water, Olea Europaea Fruit Oil, 0.25% Salicylic Acid, Lauric Acid, Stearic Acid, Sorbitol,Glycerin, Cocos Nucifera Oil, Elaeis Guineensis Oil, Botanical Acaricide, Potassium Cocoate, Lanolin, Sophora Japonica Extract, Aloe Extract, Sulfur Spring Extract, Ginseng, Coleus Forskohlii Root Oil, Tea Tree Essential Oil.

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    ROYCEDERM SULFUR SOAP. 
    sulfur soap soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82739-023
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR10 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    SORBITOL (UNII: 506T60A25R)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    LANOLIN (UNII: 7EV65EAW6H)  
    ALOE (UNII: V5VD430YW9)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    WATER (UNII: 059QF0KO0R)  
    POTASSIUM COCOATE (UNII: F8U72V8ZXP)  
    PALM OIL (UNII: 5QUO05548Z)  
    CAMPHECHLOR (UNII: 9924JQ4D5J)  
    STYPHNOLOBIUM JAPONICUM ROOT (UNII: LAH7966318)  
    4-METHYL-5-THIAZOLEETHANOL (UNII: 3XYV4I47I8)  
    OLIVE OIL (UNII: 6UYK2W1W1E)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    LAURIC ACID (UNII: 1160N9NU9U)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ASIAN GINSENG (UNII: CUQ3A77YXI)  
    COLEUS FORSKOHLII ROOT OIL (UNII: 5NXR7DJ9WO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82739-023-01232 g in 1 BOX; Type 0: Not a Combination Product09/02/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00609/02/2024
    Labeler - Shenzhen Situya Trading Co., Ltd. (706154255)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Situya Trading Co., Ltd.706154255manufacture(82739-023) , label(82739-023)