Label: CORTIZONE 10 INTENSIVE HEALING FOR ECZEMA- hydrocortisone lotion

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

Drug Label Information

Updated November 6, 2023

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

View All Sections
  • SPL UNCLASSIFIED SECTION

  • Active Ingredient:

    Hydrocortisone 1%

  • Purpose

    Anti-itch

  • Uses

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

    For external use only

    Do not use 

    • for the treatment of diaper rash. Consult a doctor.

    When using this product

    • avoid contact with 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, and do not begin use of any other hydrocortisone product unless you have asked a doctor

    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: apply to affected area not more than 3 to 4 times daily
    • children under 2 years of age: ask a doctor
  • Other information

    • contents filled by weight, not volume
  • Inactive Ingredients

    aloe barbadensis leaf juice, avena sativa (oat) kernel extract, bisabolol, boswellia serata gum, butyrospermum parkii (shea) butter extract, cetyl alcohol, dextrin, dimethicone, dipropylene glycol, disodium EDTA, glycerin, glyceryl stearate, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, isohexadecane, magnesium ascorbyl phosphate, maltodextrin, methyl gluceth-20, methylparaben, petrolatum, phenoxyethanol, polysorbate 60, propylparaben, retinyl palmitate, sodium citrate, tocopheryl acetate, water, singiber officinale (ginger) root extract (283-035) 

    *Clinically proven to moisturize for 24 hours

    **Refers to the ingredient hydrocortisone

    †Contains 7 healing moisturizers and vitamins A, C & E

  • Principal Display Panel

    NEW!

    Fast, Lasting

    Itch Relief

    MAXIMUM STRENGTH

    Cortizone-10®

    INTENSIVE HEALING

    LOTION†

    ECZEMA

    And Itchy, Dry Skin

    Dermatologist

    Recommended

    • 7 intensive moisturizers
    • Clinical strength*

     With

    Restora TM 

    Botanical &

    Vitamin Complex

    1% Hydrocortisone Anti-Itch Lotion

    DOCTORS

    #1 ITCH MEDICINE

    RECOMMEND

    Net wt 3.5 oz (99g)

    Principal Display Panel NEW! Fast, Lasting Itch Relief MAXIMUM STRENGTH Cortizone-10® INTENSIVE HEALING LOTION† ECZEMA And Itchy, Dry Skin Dermatologist Recommended  7 intensive moisturizers  Clinical strength* With Restora TM Botanical & Vitamin Complex 1% Hydrocortisone Anti-Itch Lotion DOCTORS #1 ITCH MEDICINE RECOMMEND Net wt 3.5 oz (99g)

  • INGREDIENTS AND APPEARANCE
    CORTIZONE 10 INTENSIVE HEALING FOR ECZEMA 
    hydrocortisone lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-0331
    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
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41167-0331-01 in 1 CARTON12/08/2009
    199 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01712/08/2009
    Labeler - Chattem, Inc. (003336013)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!