Label: NIZORAL SCALP ITCH RELIEF- hydrocortisone shampoo

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

Drug Label Information

Updated January 5, 2024

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

  • ACTIVE INGREDIENT

    Active ingredientPurpose
    Hydrocortisone 1.0%Anti-itch liquid
  • Uses

    • temporarily relieves itching associated with minor skin irritations, inflammation, and rashes due to:
      • eczema
      • psoriasis
      • seborrheic dermatitis
    • other uses of this product should be only under the advice and supervision of a doctor
  • WARNINGS

    Warnings
    For external use only. Use only as directed

    Flammable. Keep away from fire, or flame.

  • Do not use

    • for the treatment of diaper rash. Consult a doctor.
    • If you are allergic to any ingredient in this product
  • When using this product

    • avoid contact with the eyes
    • do not use more than directed unless told to do so by a doctor
  • Stop use and ask a doctor if

    • condition worsens, symptoms persist for more than 7 days or clear up and occur again within a few days, do not use this or any other hydrocortisone product unless you have asked a doctor.
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

  • Directions

    • twist the applicator tip to open.
    • if applying after shampooing, towel dry hair before use.
    • squeeze bottle gently to avoid excess dripping.
    • apply solution directly to scalp and massage in.
    • twist applicator tip tightly after use.
    • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
    • children under 2 years of age: do not use, ask a doctor
  • Other information

    • store product at 20-25°C (68-77°F)
    • keep carton for full product information.
  • Inactive ingredients

    alcohol denat., aloe barbadensis leaf juice, dipropylene glycol, disodium EDTA, glycerin, hyaluronic acid, menthol, PEG-12 dimethicone, phenoxyethanol and ethylhexylglycerin, polysorbate-80, tocopheryl acetate, water (aqua)

  • QUESTIONS

    Questions? 1-800-824-4894

  • PRINCIPAL DISPLAY PANEL

    Nizoral®

    Scalp Itch Relief

    HYDROCORTISONE 1%
    ANTI-ITCH LIQUID 


    RELIEVES SCALP ITCH
    from seborrheic dermatitis,
    psoriasis & eczema

    SOOTHES, CALMS & HYDRATES
    plus aloe, menthol & hyaluronic acid

    MAXIMUM STRENGTH
    anti-itch medicine

    fragrance-free • greaseless formula

    2 fl oz (60mL)

    NIZORAL®
    Scalp Itch Relief

    contains maximum strength
    medicine (Hydrocortisone
    1%) to relieve scalp itch.
    The special medicated
    solution helps soothe, calm,
    & hydrate an itchy, irritated
    scalp; plus it contains
    aloe, menthol, vitamin E
    & hyaluronic acid. The
    tapered bottle tip design
    helps easily apply the
    medicated solution that's
    paraben free, fragrance
    free, and greaseless.

    Specially 
    formulated with:

    √ Aloe
    √ Menthol
    √ Hyaluronic Acid
    √ Vitamin E

    Before use, read all label information.
    If you have a drug reaction, contact a
    doctor and report it by calling:
    1.800.824.4894

    KRAMER
    LABORITORIES

    Distributed by:
    Kramer Laboratories, Inc.
    Bridgewater, NJ 08807 USA

    © 2023 KRAMER LABORATORIES, INC.

    Nizoral Scalp Itch Relief Carton
  • INGREDIENTS AND APPEARANCE
    NIZORAL SCALP ITCH RELIEF 
    hydrocortisone shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55505-222
    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
    Alcohol (UNII: 3K9958V90M)  
    Aloe (UNII: V5VD430YW9)  
    Dipropylene Glycol (UNII: E107L85C40)  
    Edetate Disodium Anhydrous (UNII: 8NLQ36F6MM)  
    Glycerin (UNII: PDC6A3C0OX)  
    Hyaluronic Acid (UNII: S270N0TRQY)  
    Menthol, Unspecified Form (UNII: L7T10EIP3A)  
    Peg-12 Dimethicone (300 Cst) (UNII: ZEL54N6W95)  
    Phenoxyethanol (UNII: HIE492ZZ3T)  
    Ethylhexylglycerin (UNII: 147D247K3P)  
    Polysorbate 80 (UNII: 6OZP39ZG8H)  
    .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55505-222-291 in 1 CARTON01/01/2024
    160 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/01/2024
    Labeler - Kramer Laboratories (122720675)