Label: SEACALL HYDROCORTISONE OINTMENT.- seacall hydrocortisone ointment ointment

  • NDC Code(s): 76986-006-01
  • Packager: Guangdong Quadrant Ecological Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 26, 2025

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  • Active Ingredient

    HYDROCORTISONE 0.1%

  • Purpose

    Relief of dermatitis itching.

  • Use

    Used for pruritus, neurodermatitis, contact dermatitis, seborrheic dermatitis, chronic eczema.

  • Warnings

    ·For external use only.
    ·Not for infants.
    ·Use with caution in pregnant and lactating women.
    ·Prohibited for those who are allergic to this product. Allergic persons should be cautious.
    ·Prohibit the use of this product when the properties of the product have changed.
    ·Should not be used on a large scale and for a long time.

  • Do not use

    Do not use if the affected area has been broken, pus or obvious oozing or viral infections (such as herpes, blisters).

  • When Using

    When using this product, avoid contact with eyes, nose and mouth. If contact occurs, rinse thoroughly with water.

  • Stop Use

    Stop using and ask a doctor if any burning sensation, redness, or swelling at the site of application occurs or if symptoms are not relieved after 1 week of use.

  • Ask Doctor

    In case of accidental ingestion, get medical help or contact a poison control center immediately.

  • Keep Out Of Reach Of Children

    Keep out of reach of children. Children must be used under adults supervision.

  • Directions

    1~2 times a day, take a small amount of application on the affected area and gently rub for a moment.

  • Other information

    Other Information
    ·If you are using other drugs, please consult your physician or pharmacist before using this product.
    ·Athletes should use it with caution.
    ·Sealed, stored in a cool place.

  • Inactive ingredients

    MINERAL OIL,ZINC OXIDE,BEESWAX,COPERNICIA CERIFERA (CARNAUBA) WAX,POLYGLYCERYL-3 DIISOSTEARATE,TOCOPHERYL ACETATE,BISABOLOL,OCTYLDODECANOL,POLYGLYCERYL-10 DIOLEATE,BORNEOL,ECHIUM PLANTAGINEUM SEED OIL,FARNESOL,HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL UNSAPONIFIABLES,ZINGIBER OFFICINALE (GINGER) ROOT EXTRACT,CARDIOSPERMUM HALICACABUM FLOWER/LEAF/VINE EXTRACT,TOCOPHEROL

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    SEACALL HYDROCORTISONE OINTMENT. 
    seacall hydrocortisone ointment ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76986-006
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE0.1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    OCTYLDODECANOL (UNII: 461N1O614Y)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL UNSAPONIFIABLES (UNII: T7ZE2WA4MB)  
    POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)  
    POLYGLYCERYL-10 DIOLEATE (UNII: 598RES7AXX)  
    ECHIUM PLANTAGINEUM SEED OIL (UNII: PIB7XBU8XW)  
    BEESWAX (UNII: 2ZA36H0S2V)  
    FARNESOL (UNII: EB41QIU6JL)  
    GINGER (UNII: C5529G5JPQ)  
    CARDIOSPERMUM HALICACABUM FLOWERING TOP (UNII: MZP2508BRR)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    COPERNICIA CERIFERA (CARNAUBA) WAX (UNII: R12CBM0EIZ)  
    BISABOLOL (UNII: 24WE03BX2T)  
    BORNEOL (UNII: M89NIB437X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76986-006-0120 g in 1 TUBE; Type 0: Not a Combination Product05/27/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00505/27/2025
    Labeler - Guangdong Quadrant Ecological Technology Co., Ltd. (554532634)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangdong Quadrant Ecological Technology Co., Ltd.554532634manufacture(76986-006)
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