Label: AQUAX-H- hydrocortisone butyrate cream

  • NDC Code(s): 82160-127-01
  • Packager: Pella Pharmaceuticals Co. ltd
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated December 26, 2023

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

  • Composition

    Each 1 g contains: Hydrocortisone 17-Butyrate 1 mg.
    Excipients: Petrolatum, Cetearyl Alcohol, Mineral Oil, Ceteareth-20, Benzyl Alcohol, Citric Acid, Sodium Citrate, Propylparaben and Purified Water.

  • Properties

    Aquax-H ® Cream contains a corticosteroid and quickly suppresses symptoms of certain skin conditions such as itching, redness and scaling. Corticosteroids don't generally remove the cause of the symptoms. The Aquax-H ® Cream base ensures that the skin condition becomes less moist.

  • Indications

    Aquax-H ® Cream can be used for the treatment of superficial skin conditions where itching, redness and scaling are often present.

  • Contraindications

    Do not use Aquax-H ® Cream

    • If your skin condition is caused by infections with bacteria, viruses, fungi, yeasts or parasites as these could either be made worse or become unnoticeable.
    • In acne even if the skin is red.
    • For wounds or scaly skin (ichthyosis).
    • If your skin condition is the result of earlier treatment with corticosteroids such as inflammation of the skin around the mouth or thin skin possibly with streaks and vulnerable blood vessels.
    • For childhood rash on the foot sole.
    • If you are hypersensitive to hydrocortisone 17-butyrate or to any of the excipients (uncommon).
  • Precautions

    Aquax-H ®Cream contains certain excipients like Cetearyl Alcohol that in rare cases can cause hypersensitivity reactions ( itching, red spots) of the skin.

  • Drug Interactions

    Inform your doctor or pharmacist if you are using other medicines or have used them in the recent past. This also applies to medicines you have obtained without a prescription

  • Warnings

    Be extra careful with Aquax-H ® Cream

    • If you want to treat the facial skin, genital skin and skin folds as these areas of skin are particularly sensitive to corticosteroids.
    • If you apply the cream under an occlusive bandage, to large areas of skin or are treating a child in which cases you should be under the control of your doctor.
    • The Aquax-H ® Cream should not be introduced into the eye or applied to the eyelids.
    • The application of corticosteroids for long periods in children should be avoided.
    • Consult your doctor if any of the above warnings apply to you.

    Pregnancy

    Ask your doctor or pharmacist for advice before using a medical product. If you want to apply the cream during pregnancy then discuss this with your doctor.

    Breast-feeding

    Ask your doctor or pharmacist for advice before using a medical product. If you want to apply the Aquax-H ® during breast-feeding then discuss this with your doctor.

    Driving and the use of machines

    There is nothing known about Aquax-H ®Cream and the ability to drive or to use machines. However, no effects are to be expected.

  • Dosage and Administration

    Apply Aquax-H ® Cream thinly to the affected skin area and massage lightly into the skin. Do not apply more often than 1-3 times daily unless your doctor has advised otherwise.
    When your symptoms have receded, your doctor may decide that you can use the cream less often. In general, you should not use more than 1 to 2 tubes per week.
    What you can expect when treatment has been stopped
    The original symptoms can reappear if treatment is stopped prematurely.
    Always consult you doctor or pharmacist before stopping treatment.

  • Overdosage

    What you should do if you have used too much Aquax-H Cream
    Contact you doctor or pharmacist if you have used too much Aquax-H ® Cream.
    What you should do if you have forgotten to use Aquax-H Cream
    If you have forgotten to apply it a single time just carry on as before. There is no need to compensate for a missed application.

  • Side Effects

    Aquax-H ® Cream can cause side effects just like all medicines.
    You could sometimes have a burning or prickly feeling at the site of application but this is mostly not serious and disappears on its own.
    If you have used it for prolonged periods or under an occlusive bandage, you could get a rash, pimples or the formation of pus. The skin could become discolored or thin, sometimes with stripes.
    Consult your doctor if you have any of these side effects.
    Also consult your doctor or pharmacist if you either have any side effects not mentioned in this leaflet or any others that you think might be serious.

  • Storage

    Store below 25 °C
    Do not store in a refrigerator or freezer.

  • How Supplied

    30 g packs

  • THIS IS A MEDICAMENT

    • Medicament is a product which affects your health and its consumption contrary to instructions is dangerous for you.
    • Strictly follow the doctor's prescription, the method of use and the instruction of the pharmacist who sold the medicament.
    • The doctor and the pharmacist are experts in medicine, its benefits and risks.
    • Do not by yourself interrupt the period of treatment prescribed for you.
    • Do not repeat the same prescription without consulting your doctor.
    • Keep medicament out of reach of children.
  • Primary Package

    Primary Package

  • Secondary Package

    Secondary Package

  • INGREDIENTS AND APPEARANCE
    AQUAX-H 
    hydrocortisone butyrate cream
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:82160-127
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROCORTISONE BUTYRATE (UNII: 05RMF7YPWN) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE BUTYRATE30 mg  in 30 g
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82160-127-011 in 1 CARTON03/16/2015
    130 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/16/2015
    Labeler - Pella Pharmaceuticals Co. ltd (562370925)