Label: DHS SAL 4 OZ.- dhs sal shampoo

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

Drug Label Information

Updated January 1, 2024

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  • WARNINGS AND PRECAUTIONS

    For external use only. Ask a physician before use if you have Psoriasis or Seborrheic Dermatitis that covers a large area of the body. Do not get into eyes. If contact occurs, rinse eyes thoroughly with water. Stop use and ask a physician if condition worsens or does not improve after regular use.

  • Dosage and Administration

    Wet hair thoroughly. Apply a liberal amount of shampoo and massage into a rich lather. Allow lather to remain on scalp for several minutes. Rinse hair well and repeat application. For best results use at least twice a week or as directed by a physician. Store away from direct sunlight.

  • Indications and Use

    Controls crusty, flaky buildup, while relieving scalp itching and flaking, symptomatic of Psoriasis and Seborrheic Dermatitis.

  • KEEP OUT OF REACH OF CHILDREN

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

  • PURPOSE

    Controls symptoms of Psoriasis, Seborrheic Dermatitis and Dandruff

  • INACTIVE INGREDIENTS

    Purified Water

    Sodium C14-16 Olefin Sulfonate

    Triethanolamine Lauryl Sulfate

    Cocamidopropyl Betaine

    Cocamidopropyl Hydroxysultaine

    PEG 8 Distearate

  • Active Ingredient

    Salicylic Acid 35 mg/g

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    DHS Sal Shampoo.jpg image description

  • INGREDIENTS AND APPEARANCE
    DHS SAL  4 OZ.
    dhs sal shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0096-0738
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.035 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    TRIETHANOLAMINE LAURYL SULFATE (UNII: E8458C1KAA)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)  
    PEG-8 DISTEARATE (UNII: 7JNC8VN07M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0096-0738-04123.84 g in 1 BOTTLE; Type 0: Not a Combination Product06/01/1995
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03206/01/1995
    Labeler - Person and Covey (008482473)
    Establishment
    NameAddressID/FEIBusiness Operations
    Person and Covey008482473manufacture(0096-0738)
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