Label: HYDROCORTISONE CONTINUOUS- hydrocortisone aerosol, spray

  • NDC Code(s): 79481-0618-1
  • Packager: Meijer Distribution Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 13, 2024

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  • Active ingredient

    Hydrocortisone 1%

  • Purpose

    Anti-itch

  • Uses

    for the temporary relief of itching associated with minor skin irritations, inflammation, and rashes due to:

    • eczema
    • insect bites
    • poison ivy
    • poison oak
    • poison sumac
    • soaps
    • jewelry
    • detergents
    • cosmetics
    • seborrheic dermatitis
    • psoriasis
    • other uses of this product should be only under the advice and supervision of a doctor
  • Warnings

    For external use only.

    Flammable:

    Keep away from heat, sparks and open flame. Contents under pressure. Do not puncture or incinerate. Do not store at temperatures above 120 ºF. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.

    Do not use

    • for external genital, vaginal or anal itching
    • with other hydrocortisone product unless directed by a doctor
    • in or near the eyes
    • for diaper rash

    When using this product

    • avoid contact with the eyes
    • if product gets into the eye, flush with water for 15 minutes

    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 and do not begin use of any other hydrocortisone product unless you have consulted a doctor

    Keep out of the reach of children.

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

  • Directions

    • twist cap counterclockwise to unlock actuator
    • adults and children 2 years of age and older: spray affected area not more than 3 to 4 times daily
    • children under 2 years of age: do not use, consult a doctor
    • to apply to face, spray into palm of hand and gently apply
  • Inactive ingredients

    aloe barbadensis leaf juice, avena sativa (oat) kernel extract, citric acid, disodium EDTA, ethoxydiglycol, glycerin, maltodextrin, menthyl lactate, methyl gluceth-20, PEG-8, SD alcohol 40-B, sodium citrate, water

  • Questions ?

    Call 1-866-964-0939

  • Principal Display Panel

    meijer

    Maximum Strength

    hydrocortisone

    spray

    HYDROCORTISONE 1%/ANTI-ITCH

    Relieves Itching

    Maximum Strength

    Relieves itching from

    rashes, irritation,

    insect bites &

    poison ivy,

    oak & sumac

    No-touch & no-mess

    NET WT 4.0 0Z (113 g)

    image 1

  • INGREDIENTS AND APPEARANCE
    HYDROCORTISONE CONTINUOUS 
    hydrocortisone aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79481-0618
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE10 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    METHYL GLUCETH-20 (UNII: J3QD0LD11P)  
    OAT (UNII: Z6J799EAJK)  
    WATER (UNII: 059QF0KO0R)  
    DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
    ALCOHOL (UNII: 3K9958V90M)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79481-0618-1113 g in 1 CAN; Type 0: Not a Combination Product08/27/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01708/27/2023
    Labeler - Meijer Distribution Inc. (006959555)
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