Label: WALGREENS- salicylic acid lotion/shampoo

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated November 2, 2022

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  • ACTIVE INGREDIENT

    Salicylic Acid 3%

  • PURPOSE

    Dandruff control

  • INDICATIONS & USAGE

    Controls flaking , scaling and itching from dandruff

  • WARNINGS

    For external use only

    • on scalp that is broken or inflammed
    • if you are allergic to ingredients in 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 centre immediately .
  • DOSAGE & ADMINISTRATION

    • For maximum dandruff control, use every time you shampoo.
    • wet hair, massage onto scalp and rinse.
    • Repeat if desired.
  • STORAGE AND HANDLING

    Store at room temperature.

  • INACTIVE INGREDIENT

    Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Panthenol, Ascrobic Acid, Camellia Sinensis Leaf Extract, PEG-120 Methyl Glucose Dioleate, Linoleamidopropyl PG-Dimonium Chloride Phosphate, Polyquaternium-7, Fragrance (parfum), Tocopheryl Acetate, Sodium Hydroxide

  • PRINCIPAL DISPLAY PANEL

    7 oz

  • INGREDIENTS AND APPEARANCE
    WALGREENS 
    salicylic acid lotion/shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-9536
    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
    POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)  
    FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17)  
    .ALPHA.-TOCOPHERYLOXYACETIC ACID (UNII: JW7FJR3ZLY)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    LINOLEAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: 5Q87K461JO)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-9536-07207 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 finalM03211/02/2022
    Labeler - Walgreens (008965063)
    Registrant - Apollo Health and Beauty Care (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apollo Health and Beauty Care201901209manufacture(0363-9536)
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