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Prednisolone 0.625 mg/0.1 Gm To 7.5 mg/0.1 Gm Topical Lipoderm® (Vet)

FDA-approved generic
Dose form
Topical Gel
Active ingredients
Prednisolone

Prednisolone Topical Lipoderm® (Vet) is a semisolid formulation used for the treatment of various skin conditions in animals such as Atopic Dermatitis, Allergic Dermatitis, Pruritus, Pyoderma, and Intertrigo. The medication is dispensed through a pump mechanism for easy and precise application. It is available in strengths ranging from 0.625 mg/0.1 Gm to 7.5 mg/0.1 Gm.

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For prescribers
Prescription details
RxThis formula
Dose formSee below
Quantity____
SigAs directed by prescriber
Refills____
PharmacyBayview Pharmacy, Warwick RI, NCPDP 4106882
Copy prescription detailsOrder form
Controlled substance: e-prescribe (EPCS) from your EHR. Faxed and phoned prescriptions cannot be accepted for this preparation.
Send it from your EHR, or fax to (401) 284-4506. How to e-prescribe this formula
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.
To prescribe, you must be a verified prescriber.
To prescribe, you must be in a state where we hold an active out-of-state pharmacy license.
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This medication requires a prescription from your doctor

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.

For prescribersSign in for prescription details and order forms.
Compounded preparations are prepared by Bayview pursuant to a prescription for an individual patient. They are not FDA-approved and have not been evaluated by FDA for safety or effectiveness.
Prednisolone
Topical Gel
6427079ea643242d545190e9

Formula Information

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Bayview Pharmacy is pleased to provide Prednisolone 0.625 mg/0.1 Gm To 7.5 mg/0.1 Gm Topical Lipoderm® (Vet) as a specially compounded topical medication designed for the treatment of various disease states. This unique formulation combines the anti-inflammatory and swelling reduction properties of prednisolone with the enhanced absorption capabilities of Lipoderm®, a specialized topical delivery system.

This compounded formulation is utilized in the treatment of a wide range of conditions, including but not limited to skin inflammation, allergies, and dermatitis. The formulation is particularly beneficial for patients with sensitive skin, as it is designed to minimize irritation and inflammation.

The Prednisolone 0.625 mg/0.1 Gm To 7.5 mg/0.1 Gm Topical Lipoderm® (Vet) formulation is available in a range of strengths, from 0.625 mg/0.1 Gm to 7.5 mg/0.1 Gm. The appropriate strength of the formulation is determined by the prescriber, taking into account the specific needs of the individual patient.

What sets this formulation apart is its semisolid state, dispensed through a pump mechanism. This allows for easy and precise application on the skin, ensuring targeted treatment or absorption of active ingredients. The gel-like consistency of the formulation further aids in the ease of application and absorption.

If you have any questions about this Prednisolone 0.625 mg/0.1 Gm To 7.5 mg/0.1 Gm Topical Lipoderm® (Vet) formulation or its potential uses in treating various disease states, please do not hesitate to contact us at Bayview Pharmacy. Our team of compounding pharmacists is ready and willing to assist you with any queries you may have.

Drug Interactions

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Prednisolone 0.625 mg/0.1 Gm To 7.5 mg/0.1 Gm Topical Lipoderm® (Vet) is a compounded formulation designed for the treatment of various skin conditions in animals. These conditions may include eczema, psoriasis, dermatitis, and allergic reactions. Prednisolone, the active ingredient, is a corticosteroid that functions by reducing inflammation and suppressing the immune system.

It is crucial to understand that this formulation should not be used for more than two weeks due to potential side effects. These may include skin thinning, stretch marks, and acne. Additionally, this formulation may cause irritation or burning at the application site. Therefore, it is important to monitor the treated area and report any adverse reactions to your veterinarian promptly.

When applying Prednisolone 0.625 mg/0.1 Gm To 7.5 mg/0.1 Gm Topical Lipoderm® (Vet), avoid contact with the eyes, nose, and mouth of the animal. Always wash your hands after application to prevent accidental ingestion or contact with sensitive areas. It is also important to note that this formulation may interact with other medications, such as antibiotics, antifungals, and other topical medications. Therefore, always inform your veterinarian of any other medications your pet is currently taking before using this formulation.

If you have any questions or concerns about Prednisolone 0.625 mg/0.1 Gm To 7.5 mg/0.1 Gm Topical Lipoderm® (Vet) or its potential interactions, do not hesitate to reach out to your veterinarian or a trusted healthcare professional. They can provide you with the most accurate and relevant information based on your pet's specific health condition and needs.

How Does it Work

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Prednisolone 0.625 mg/0.1 Gm To 7.5 mg/0.1 Gm Topical Lipoderm® (Vet) is a compounded formulation designed to treat a variety of skin conditions in animals. This topical corticosteroid combines the anti-inflammatory and immune-suppressing properties of prednisolone with Lipoderm®, a proprietary blend of lipids and emollients. The Lipoderm® component enhances the penetration of prednisolone into the skin, thereby increasing its effectiveness.

The formulation is available in a range of strengths, from 0.625 mg/0.1 Gm to 7.5 mg/0.1 Gm, allowing for customization based on the severity of the condition being treated. It is dispensed through a pump mechanism, which facilitates easy and precise application on the skin. The formulation should be applied directly to the affected area, typically once or twice daily, as per the instructions provided by your veterinarian.

It can also be used to treat skin conditions caused by parasites, such as mange. The formulation works by reducing inflammation, itching, and redness associated with these conditions.

If you have any questions about Prednisolone 0.625 mg/0.1 Gm To 7.5 mg/0.1 Gm Topical Lipoderm® (Vet) or its use in treating your pet’s skin condition, please do not hesitate to reach out. We are here to provide the necessary guidance and support.

Other Uses

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Prednisolone 0.625 mg/0.1 Gm To 7.5 mg/0.1 Gm Topical Lipoderm® (Vet) is a versatile compounded formulation that can be used to treat a wide range of skin conditions. This formulation can also be used to alleviate discomfort from insect bites, stings, and other minor skin irritations.

Furthermore, Prednisolone 0.625 mg/0.1 Gm To 7.5 mg/0.1 Gm Topical Lipoderm® (Vet) can be used to manage inflammation and itching associated with certain autoimmune disorders, such as lupus and rheumatoid arthritis.

For those suffering from allergic reactions, such as hives and eczema, Prednisolone 0.625 mg/0.1 Gm To 7.5 mg/0.1 Gm Topical Lipoderm® (Vet) can provide relief from inflammation and itching. It can also be used to manage skin conditions like rosacea and acne, as well as dermatitis herpetiformis and lichen planus.

If you have any questions about the use of Prednisolone 0.625 mg/0.1 Gm To 7.5 mg/0.1 Gm Topical Lipoderm® (Vet) for any of these conditions, please do not hesitate to reach out for more information.

Frequently Asked Questions

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What is Prednisolone 0.625 mg/0.1 Gm To 7.5 mg/0.1 Gm Topical Lipoderm® (Vet)?

This is a semisolid formulation of Prednisolone, a corticosteroid, dispensed through a pump mechanism. It is designed for easy and precise application on the skin for targeted treatment or absorption of active ingredients.

What is the consistency of this Prednisolone formulation?

The Prednisolone formulation is in a gel-like consistency, which makes it easy to apply on the skin.

How is the Prednisolone formulation applied?

The formulation is dispensed through a pump mechanism, which facilitates easy and precise application on the skin.

What is the purpose of the pump mechanism in this formulation?

The pump mechanism allows for easy and precise application of the formulation on the skin, ensuring that the correct dosage is applied each time.

Is this Prednisolone formulation for human or veterinary use?

This particular formulation of Prednisolone is intended for veterinary use.

What is the active ingredient in this Prednisolone formulation?

The active ingredient in this formulation is Prednisolone, a corticosteroid that is used to treat a variety of conditions in animals.

What is the benefit of the gel-like consistency of this formulation?

The gel-like consistency of this formulation allows for easy application and absorption of the active ingredients into the skin.

Can this Prednisolone formulation be used for all animals?

As with any medication, it's important to consult with a veterinarian before using this Prednisolone formulation on your pet. The vet will be able to determine if this medication is suitable for your pet's specific condition and needs.

How should this Prednisolone formulation be stored?

It's recommended to store this formulation in a cool, dry place away from direct sunlight. Always keep it out of reach of children and pets.

What should I do if my pet has an adverse reaction to this Prednisolone formulation?

If your pet has an adverse reaction to this formulation, such as skin irritation or other symptoms, stop using the product and consult with your veterinarian immediately.

About this compounded preparation

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.

Formulas and/or material listed are not to be interpreted as a promise, guarantee or claim of therapeutic efficacy or safety. The information contained herein is not intended to replace or substitute for conventional medical care, or encourage its abandonment. Every patient is unique, and formulas should be adjusted to meet their individual needs.

No compounded medications are reviewed by the FDA for safety or efficacy.
For prescribers

How to e-prescribe this formula

Controlled substance: e-prescribe only (EPCS). Faxed, phoned, and handwritten prescriptions cannot be filled. Rhode Island law (R.I. Gen. Laws § 21-28-3.18) requires Schedule II to V prescriptions to be transmitted electronically.
1

Find Bayview in your EHR's pharmacy directory

Search by NCPDP 4106882, or by name and ZIP: Bayview Pharmacy, Warwick, RI 02886. Select it as the destination pharmacy and save it as a favorite. Click any value to copy it.

NCPDP4106882NPI1750455143Address3844 Post Rd, Warwick, RI 02886Phone(401) 284-4505Fax(401) 284-4506
2

Enter the formula as a compound

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.

3

Copy the prescription details

RxFormula name
Dose formDose form
Quantity________
SigAs directed by prescriber
Refills____
PharmacyBayview Pharmacy, Warwick RI, NCPDP 4106882
Copy prescription details

Quantity and directions are starting points for this dose form, not treatment recommendations. Dosing remains the prescriber's responsibility.

4

Send it

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.

Do not use Notes to Pharmacy for the formula. Some EHRs keep that field internal and never transmit it. A prescription that arrives without the formula is delayed while we call your office.

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.

Prednisolone 0.625 mg/0.1 Gm To 7.5 mg/0.1 Gm Topical Lipoderm® (Vet)
Topical Gel
60 g
controlled

Apply topically to affected area(s)

Twice daily, apply 0.625 mg/ 0.1 gm-7.5 mg/0.1 gm Topical Lipoderm® (Vet) to affected area(s).