Label: HAIRCARE PHYSICIANS RECOMMENDED- salicylic acid shampoo

  • NDC Code(s): 82499-267-00
  • Packager: LAWRENCE E SAMUELS MD INC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 11, 2023

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

  • Drug Facts

  • Active ingredients

    Salicylic Acid 3.00 %

    Purpose

    dandruff, seborrheic

    dermatitis, psoriasis

  • Uses:

    • Controls the symptoms of dandruff, seborrheic dermatitis, and psoriasis.
  • Warnings:

    For external use only.

    When using this product

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

    Ask a doctor before using this product if

    • condition covers a large area of the body

    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.

    If pregnant or breast-feeding,

    ask a health professional before use

  • Directions:

    • For best results use at least twice a week or as directed by a doctor.
    • Wet hair thoroughly.
    • Massage liberal amount of shampoo into the scalp. 
    • Leave lather on scalp for several minutes.
    • Rinse and repeat.
  • Inactive ingredients:

    Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water),Cocamide MEA, Cocamidopropyl Betaine, Disodium Oleamide MEA-Sulfosuccinate, Ethylhexylglycerin, Glycerin, Glycol Stearate, Glycolic Acid, Guar Hydroxypropyltrimonium Chloride, Isostearamidopropyl Morpholine Lactate, Lauramine Oxide, a-Lipoic Acid, Parfum (Fragrance), Phenoxyethanol, Sodium Hydroxide, Sodium Laureth Sulfate, Sodium Lauryl Sulfate, Triethanolamine 

  • Questions?

    314-205-8300

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    HAIRCARE PHYSICIANS RECOMMENDED 
    salicylic acid shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82499-267
    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
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    DISODIUM OLEAMIDO MONOETHANOLAMINE SULFOSUCCINATE (UNII: 5M1101WGSY)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCOL STEARATE (UNII: 0324G66D0E)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)  
    ISOSTEARAMIDOPROPYL MORPHOLINE LACTATE (UNII: 082Y3WQI5K)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82499-267-00237 mL in 1 BOTTLE; Type 0: Not a Combination Product01/15/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03201/15/2022
    Labeler - LAWRENCE E SAMUELS MD INC (006119481)