Label: AQUAPHOR ITCH RELIEF- hydrocortisone ointment

  • NDC Code(s): 10356-120-04, 10356-120-07, 10356-120-30, 10356-120-52, view more
    10356-120-53, 10356-120-54
  • Packager: Beiersdorf Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 28, 2023

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  • ACTIVE INGREDIENT

    Active Ingredient

    Hydrocortisone 1%

  • PURPOSE

    Purpose

    Anti-Itch Ointment

  • INDICATIONS & USAGE

    Uses

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

    • eczema
    • insect bites
    • soaps
    • poison ivy, oak, sumac
    • seborrheic dermatitis
    • psoriasis
    • detergents
    • cosmetics
    • jewelry

  • WARNINGS

    Warnings

    For external use only

  • DO NOT USE

    Do not use
    • for the treatment of diaper rash. Consult a doctor.

  • WHEN USING

    When using this product
    • avoid contact with eyes
    • do not exceed the recommended daily dosage unless directed by a doctor

  • STOP USE

    Stop use and consult a doctor if
    • condition worsens, if 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

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

  • DOSAGE & ADMINISTRATION

    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: Do not use, consult a doctor.

  • INACTIVE INGREDIENT

    Inactive ingredients

    Petrolatum, Mineral Oil, Ceresin, Lanolin Alcohol,
    Panthenol, Glycerin, Bisabolol, Menthoxypropanediol

  • QUESTIONS

    Questions or comments?
    1-800-227-4703

  • PRINCIPAL DISPLAY PANEL

    Aquaphor Itch Relief Ointment

    Maximum Strength

    Immediately Soothes & Relieves Itch & Irritiation

    Up to 12 hours Significant Itch Relief

    Clinically Proven

    1% Hydrocortisone Anti-Itch Ointment

    Dermatologist Recommended Brand

    Fragrance free and Paraben free

    Hypoallergenic

    Helps Heal the Itch

    Clinically proven significant itch relief for up to 12 hours

    Immediately soothes itchy spots to help skin heal

    Skin irritation

    Skin rashes

    Eczema

    Psoriasis

    Eczema

    Poison Ivy

    aqitchreliefcarton

    Children's

    Aquaphor Itch Relief Ointment

    Ages 2 Years and Older

    Immediately Soothes & Relieves Itch & Irritiation

    Up to 12 hours Significant Itch Relief

    Clinically Proven

    Number 1 Pediatrician Recommended Brand for Eczema

    1% Hydrocortisone Anti-Itch Ointment

    Dermatologist Recommended Brand

    Fragrance free and Paraben free

    Hypoallergenic

    Helps Heal the Itch

    Clinically proven significant itch relief for up to 12 hours

    Immediately soothes itchy spots to help skin heal

    Eczema

    Skin irritation

    Skin rashes

    Psoriasis

    Eczema

    Poison Ivy

    aqchilditchreliefcarton

  • INGREDIENTS AND APPEARANCE
    AQUAPHOR ITCH RELIEF 
    hydrocortisone ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10356-120
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    3-((L-MENTHYL)OXY)PROPANE-1,2-DIOL (UNII: KD6TZ2QICH)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    CERESIN (UNII: Q1LS2UJO3A)  
    LANOLIN ALCOHOLS (UNII: 884C3FA9HE)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    LEVOMENOL (UNII: 24WE03BX2T)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10356-120-300.9 g in 1 PACKET; Type 0: Not a Combination Product11/01/2020
    2NDC:10356-120-521 in 1 CARTON11/01/2020
    2NDC:10356-120-0428 g in 1 TUBE; Type 0: Not a Combination Product
    3NDC:10356-120-0428 g in 1 TUBE; Type 0: Not a Combination Product11/01/2020
    4NDC:10356-120-532 in 1 CARTON11/01/2020
    4NDC:10356-120-0428 g in 1 TUBE; Type 0: Not a Combination Product
    5NDC:10356-120-541 in 1 CARTON06/01/2021
    5NDC:10356-120-0756 g in 1 TUBE; Type 0: Not a Combination Product
    6NDC:10356-120-0756 g in 1 TUBE; Type 0: Not a Combination Product06/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01711/01/2020
    Labeler - Beiersdorf Inc (001177906)
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