Label: TOTAL RELIEF- hydrocortisone shampoo

  • NDC Code(s): 71516-342-00
  • Packager: DR. MARDER SKINCARE, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 11, 2023

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  • Drug Facts

  • Active Ingredient

    Hydrocortisone 1%

    Purpose

    Anti-itch liquid

  • Uses:

    helps control the symptoms of scalp itch associated with minor skin irritations and rashes due to

    • Seborrheic Dermatitis
    • Eczema
    • Psoriasis
  • Warnings:

    For external use only.

    When using this product

    avoid contact with eyes

    Stop use and ask a doctor

    if condition worsens, symptoms persist for more than 7 days or clear up and occur again.

    Keep out of reach of children.

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

  • Directions:

    • Adults and children 2 years of age and older: Wet hair thoroughly. Apply shampoo, generously lather scalp for several minutes. Rinse thoroughly, Repeat.
    • Follow with Step 2 Total Relief Conditioner
    • Use daily if needed.
  • Other Information

    • store at room temp. 20° - 25° C (68° - 77° F)
  • Inactive ingredients

    Aqua (Deionized Water), Ascorbic Acid (Vitamin C), Biotin, Caffeine, Camellia Sinensis (Green Tea) Leaf Extract, Caprylyl Glycol, Cocamidopropyl Betaine, Cocos Nucifera (Coconut) Oil, Decyl Glucoside, dl-Panthenol, Glycerin, Glycol Stearate, Hexylene Glycol, Lauryl Glucoside, Lecithin, Methylisothiazolinone, Parfum (Fragrance), Phenoxyethanol, Potassium Sorbate, Propylene Glycol, Resveratrol, Retinyl Palmitate (Vitamin A), Sodium C14-C16 Olefin Sulfonate, Sodium Metabisulfite, Tocopheryl Acetate (Vitamin E), Xanthan Gum

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    TOTAL RELIEF 
    hydrocortisone shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71516-342
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    BIOTIN (UNII: 6SO6U10H04)  
    CAFFEINE (UNII: 3G6A5W338E)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCOL STEARATE (UNII: 0324G66D0E)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    RESVERATROL (UNII: Q369O8926L)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71516-342-00180 mL in 1 TUBE; Type 0: Not a Combination Product07/25/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01707/25/2022
    Labeler - DR. MARDER SKINCARE, LLC (146890103)
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