Label: WALGREENS- salicylic acid lotion/shampoo

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

Drug Label Information

Updated February 22, 2024

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  • ACTIVE INGREDIENT

    Salicylic Acid -3 %

  • Purpose

    psoriasis and seborrheic dermatitis

  • Uses

    Used topically to control seborrheic dermatitis and psoriasis of the scalp.

  • Warnings

    For external use only

    As a doctor before use if

    • If condition covers a large area of the body.
    • If you are allergic to ingredients in this product.

    When using this product

    • Avoid contact with eyes.
    • If contact occurs, rinse thoroughly with water.

    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

    • In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.
  • Directions

    • For best results, use at least twice weekly or as directed by clinician
    • Apply to wet skin and/or scalp and massage to form a lather
    • Leave lather on for several minutes.
    • Rinse thoroughly and repeat if necessary.
  • Other information

    • Store at room temperature
  • Inactive Ingredients

    Water (Aqua), C 14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Panthenol, Ascorbic Acid, Camellia Sinensis Leaf Extract, PEG-120 Methyl Glucose Dioleate, Linoleamidopropyl PG-Dimonium Chloride Phosphate, Polyquaternium-7, Melaleuca Aternifolia (Tea Tree) Leaf Oil, Tocopheryl Acetate, Sodium Hydroxide.

  • Questions???

    1-800-925-4733

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  • INGREDIENTS AND APPEARANCE
    WALGREENS 
    salicylic acid lotion/shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-9537
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID30 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    CAMELLIA SINENSIS ROOT (UNII: 8H54O0V2K3)  
    LINOLEAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: 5Q87K461JO)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 900 KD) (UNII: B70CUU14M9)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-9537-11325 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/02/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03211/02/2022
    Labeler - Walgreens (008965063)
    Registrant - Apollo Health and Beauty Care (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apollo Health and Beauty Care201901209manufacture(0363-9537)
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