This Hydrocortisone 1% and Zinc Oxide 0.5% suppository formulation is a solid dosage form designed for insertion into a body cavity, typically the rectum or vagina. Upon dissolution or melting, it releases medication for local or systemic absorption. It is commonly used to treat conditions such as diaper rash, hemorrhoids, pruritus ani, anal fissures, and perianal dermatitis.

Licensed to fill prescriptions for patients in RI, MA, CT, NJ, NH, FL, ME and PA. New York patients are served on a limited basis while nonresident registration is pending.
Hydrocortisone 1%/Zinc Oxide 0.5% Suppository is a specially compounded medication designed to treat a range of skin conditions. This unique formulation combines hydrocortisone, a potent corticosteroid, and zinc oxide, a known anti-inflammatory agent.
The suppository form of this medication offers a number of advantages over traditional topical creams or ointments. It is easy to use and provides a more direct delivery of the active ingredients to the affected area. This direct delivery system allows for a more targeted treatment approach, reducing the need for frequent application and increasing the overall effectiveness of the medication.
The hydrocortisone in this formulation works to reduce inflammation and itching, providing immediate relief from discomfort. The zinc oxide component serves to protect the skin from further irritation, creating a protective barrier that aids in the healing process. This combination of ingredients not only reduces the symptoms of the skin condition but also promotes healing, providing a comprehensive treatment approach.
As with all medications, it is crucial to use this formulation as directed by your healthcare provider. If you have any questions or concerns about this formulation, we encourage you to reach out to us at Bayview Pharmacy. We are here to provide the support and guidance you need to ensure you get the most out of your treatment.
This Hydrocortisone 1%/Zinc Oxide 0.5% Suppository formulation is a solid dosage form designed for insertion into a body cavity, typically the rectum or vagina. Upon insertion, it dissolves or melts to release medication for local or systemic absorption. It is primarily used for the treatment of various inflammatory and pruritic skin conditions, including eczema, psoriasis, and contact dermatitis. Additionally, it can be used to treat diaper rash and other skin irritations.
Patients should be aware that this formulation may cause local irritation, burning, or itching. If these symptoms occur, it is recommended to discontinue use and contact a healthcare provider. Furthermore, this formulation may cause skin discoloration or staining. It is important to note that this formulation should not be used for the treatment of any other conditions.
There may be potential interactions with other medications, including topical corticosteroids, topical antibiotics, and antifungal medications. Therefore, patients should inform their healthcare provider of any other medications they are currently taking before using this formulation.
Prescribers should also be aware of the potential side effects and interactions of this formulation. If patients report symptoms such as local irritation, burning, or itching, it is recommended to discontinue use and seek medical advice. Prescribers should also inform their patients about the potential for skin discoloration or staining.
It is crucial for prescribers to be aware of potential interactions with other medications, including topical corticosteroids, topical antibiotics, and antifungal medications. Therefore, prescribers should ensure their patients are fully informed about any other medications they are taking before using this formulation.
If you have any questions about this formulation or its interactions, please do not hesitate to reach out for further information.
This Hydrocortisone 1%/Zinc Oxide 0.5% Suppository formulation is a compounded medication designed to treat a range of skin conditions such as eczema, psoriasis, and diaper rash. The combination of hydrocortisone and zinc oxide works synergistically to alleviate inflammation and irritation. Hydrocortisone specifically targets the itching and redness associated with these skin conditions, while zinc oxide serves as a protective barrier to prevent further irritation.
The suppository is a solid dosage form that is inserted into the rectum, where it dissolves or melts to release the medication. This allows for local or systemic absorption, depending on the specific treatment needs. It is crucial to use this medication as directed by your healthcare provider, ensuring not to exceed the recommended dosage. The duration of use should also align with the prescribed period given by your healthcare provider.
It is important to remember that this formulation should not be applied to broken or infected skin. If you experience any adverse reactions such as burning, itching, or irritation, discontinue use immediately and consult with your healthcare provider. Always ensure to follow the instructions carefully to achieve the best possible therapeutic outcomes.
If you have any queries or concerns about this Hydrocortisone 1%/Zinc Oxide 0.5% Suppository formulation or its application, do not hesitate to contact your healthcare provider or pharmacist. They can provide you with the necessary guidance and advice to ensure safe and appropriate use of this medication.
This Hydrocortisone 1%/Zinc Oxide 0.5% Suppository formulation is a versatile treatment option for a range of conditions. The suppository works by reducing inflammation and irritation in the anal area, providing relief from discomfort. It also plays a crucial role in minimizing the risk of infection in the anal region, thereby preventing further irritation and inflammation.
Moreover, this formulation is beneficial in alleviating symptoms such as anal itching, burning, and pain. It is also instrumental in reducing the risk of developing anal abscesses and fistulas, conditions that can cause severe pain and discomfort if left untreated. Furthermore, this formulation can be used as a preventive measure against anal cancer.
If you have any queries or concerns regarding the use of this Hydrocortisone 1%/Zinc Oxide 0.5% Suppository formulation, please do not hesitate to contact us.
A Hydrocortisone 1%/Zinc Oxide 0.5% Suppository is a solid dosage form of medication that is inserted into a body cavity, typically the rectum or vagina. It dissolves or melts to release the medication for local or systemic absorption.
Once inserted, the suppository dissolves or melts, releasing the Hydrocortisone and Zinc Oxide. These active ingredients then work to reduce inflammation and irritation in the affected area.
You should insert the suppository into the rectum or vagina as directed by your healthcare provider. It is typically used once or twice a day, depending on the severity of your symptoms.
Some potential side effects include irritation or burning at the site of application. If these side effects persist or worsen, contact your healthcare provider immediately.
Consult your healthcare provider before using this medication if you are pregnant or breastfeeding. They will be able to advise you on the best course of action based on your individual circumstances.
This medication should only be used by children if prescribed by a healthcare provider. Always follow the provider's instructions carefully when administering medication to children.
If you miss a dose, use it as soon as you remember. If it is near the time of the next dose, skip the missed dose and resume your usual dosing schedule. Do not double the dose to catch up.
Before starting any new medication, including over-the-counter drugs and dietary supplements, discuss it with your healthcare provider or pharmacist. Some products may interact with Hydrocortisone 1%/Zinc Oxide 0.5% Suppository, affecting how it works.
Store this medication at room temperature, away from light and moisture. Do not store in the bathroom. Keep all medications away from children and pets.
If someone has overdosed and has serious symptoms such as passing out or trouble breathing, call emergency services immediately. Otherwise, call a poison control center right away.
This formulation is compounded by Bayview Pharmacy on a prescriber's order for an individual patient. It is not an FDA-approved drug product, and the FDA has not evaluated it for safety, effectiveness, or manufacturing quality.
The conditions listed on this page are indications prescribers have ordered this preparation for. They are not FDA-approved indications, and listing them is not a statement that this preparation is effective for them.
A valid prescription is required. Availability depends on Bayview's licensure in your state. This page is general information, not medical advice — discuss your situation with a licensed healthcare provider.
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Compounded preparations have no NDC, so this formula will not appear in your EHR's drug search. Use your system's compound, non-formulary, or free-text prescription entry and name the preparation exactly as written in step 3. If your EHR forces you to pick a listed drug, pick the closest entry for the active ingredient and put the full formula in the prescription body (the Sig or directions field), not in Notes to Pharmacy.
Compounded preparations have no NDC and will not appear in your drug search. For EPCS to validate, select a drug entry your EHR recognizes as controlled, usually the bulk powder entry for the active ingredient (for example Ketamine (bulk) powder, not a branded product), then put the full formula from step 3 in the prescription body. A free-text entry that does not validate as controlled will be rejected by your EPCS module.
Quantity and directions are starting points for this dose form, not treatment recommendations. Dosing remains the prescriber's responsibility.
Transmit from your EHR. For this non-controlled preparation we also accept fax to (401) 284-4506 and phoned orders at (401) 284-4505. Order forms are on the formulation pages and in the prescriber portal.
Transmit with two-factor authentication through your EPCS-enabled EHR. No order form is offered for this preparation; e-prescribing guides for our controlled preparations are on the formulation pages.
Licensed to dispense in RI, MA, CT, NJ, NH, FL, ME, and PA; New York is served on a limited basis while nonresident registration is pending. Compounded preparations are not FDA-approved. A valid prescription is required. Full guide, including steps by EHR: How to e-prescribe to Bayview. Questions about this formula: call (401) 284-4505.
Insert 1 unwrapped suppository