Label: SORARESAL- salicylic acid cream

  • NDC Code(s): 73526-002-02, 73526-002-06
  • Packager: Summer Herbal Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 6, 2023

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

  • Drug Facts

  • Active ingredient

    Salicylic acid 2%

  • Purpose

    Psoriasis

  • Use

    for relief of the symptoms of psoriasis.

  • Warnings

    For external use only.

    Do not use

    • on open wounds, infected or cracked skin.

    • if you are sensitive or allergic to any of the ingredients used in this product.

    Ask a doctor before use if you have a condition that covers a large area of the body.

    When using this product

    • avoid contact with the eyes and if contact occurs, rinse eyes thoroughly with water.

    • avoid contact with the mouth, genitals and mucous membranes.

    • avoid direct sunlight after use.

    Stop use and ask a doctor if

    • condition worsens or does not improve after regular use of this product as directed.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • gently apply a layer to affected areas one to three times daily or as directed by a doctor.

    • please allow the cream to stay in contact with your skin for as much time as possible to have full absorption before reapplying.

  • Other information

    Store in a cool dark place at room temperature at 68°F - 77°F.

  • Inactive ingredients

    Water (Aqua), Safflower (Carthamus tinctorius) Seed, Banyan Tree (Ficus benghalensis) Bark, Golden Shower Tree (Cassia fistula) Whole plant, Coconut (Cocos nucifera) Oil, Glycerin, Glyceryl Monostearate, Polysorbate 80, Cetostearyl Alcohol, Cetyl Palmitate, Stearic Acid, Cetyl Alcohol, Triethanolamine, Phenoxyethanol, Dimethicone, Butylated Hydroxyanisole, Butylated Hydroxytoluene.

  • Questions or comments?

    1-800-743-1718

    Mon-Fri 9:00 A.M. - 5:00 P.M.

  • SPL UNCLASSIFIED SECTION

    FOR PSORIASIS 

    with 2% Salicylic Acid

    • Controls Recurrence

    • Relieves Itching

    • Reduces Scaling

    • Dermo-Cosmetic

    • 100% Steroid-Free

    • No Added Fragrance

    Distributed by:
    SUMMER HERBAL INC., 510 Saint Johns Court,
    Oak Brook, IL 60523

    You may report serious side effects to the above U.S. address.

    PRODUCT OF INDIA

    Soraresal Cream relieves itching, calms irritation and reduces scaling for easy relief from psoriasis. The active ingredient of 2% salicylic acid effectively makes your skin clear. Sustainably harvested plants, beautify and moisturize the skin with powerful oils. Control psoriasis easily with Soraresal.

    Manufactured for:
    Atrimed Pharmaceuticals Pvt. Ltd.

    Manufactured By:
    BioMylz Pvt. Ltd.
    at Building No. 1, # 21-D, 2nd Phase
    Peenya Industrial Area
    Bangalore, Karnataka 560058, India

  • Packaging

    SorSalcy-1SorSalcy-2

  • INGREDIENTS AND APPEARANCE
    SORARESAL 
    salicylic acid cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73526-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SAFFLOWER OIL (UNII: 65UEH262IS)  
    FICUS BENGHALENSIS BARK (UNII: S7NJY6RN0N)  
    CASSIA FISTULA WHOLE (UNII: LS6U4E0H5H)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETYL PALMITATE (UNII: 5ZA2S6B08X)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73526-002-061 in 1 BOX09/16/2020
    1191 g in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:73526-002-021 in 1 BOX10/01/2021
    250 g in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03201/01/2020
    Labeler - Summer Herbal Inc. (053442867)