The Gabapentin 6%/Mometasone Furoate 0.1% Topical Gel is a specialized semisolid formulation designed for targeted skin application. This unique preparation combines the nerve pain relief properties of Gabapentin with the potent anti-inflammatory and immunosuppressive effects of Mometasone Furoate. The gel is dispensed through a pump mechanism, which ensures ease of use and precise dosing. Its gel-like consistency allows for smooth application and potential enhanced absorption of the active ingredients into the skin.
This formulation is primarily used to treat localized neuropathic pain, which may be associated with conditions such as postherpetic neuralgia or diabetic neuropathy. Additionally, the inclusion of Mometasone Furoate makes it suitable for addressing inflammatory skin conditions, such as eczema or psoriasis, where both pain relief and anti-inflammatory action are desired. The combination of these two active ingredients in a topical gel form provides a synergistic approach to managing symptoms associated with these disease states.

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.
The Gabapentin 6%/Mometasone Furoate 0.1% Topical Gel is a specialized semisolid formulation designed for targeted application on the skin. This unique combination of an anticonvulsant and a corticosteroid is dispensed through a pump mechanism, which ensures ease of use and precise dosing. The gel base provides a suitable medium for the active ingredients to be absorbed into the skin, offering both local and systemic therapeutic effects.
In this formulation, Gabapentin acts locally to reduce pain signaling and inflammation without significant systemic absorption, thereby minimizing potential systemic side effects.
Mometasone Furoate is a potent corticosteroid with anti-inflammatory, antipruritic, and vasoconstrictive properties. At a concentration of 0.1%, it is used to treat various dermatological conditions, including but not limited to eczema, psoriasis, and allergic reactions. The inclusion of Mometasone Furoate in this gel formulation helps to reduce the inflammation and itching that can be associated with these skin conditions, providing relief and aiding in the healing process.
The combination of Gabapentin and Mometasone Furoate in a topical gel form is particularly beneficial for patients who require localized treatment with minimal systemic exposure. This can be advantageous in managing conditions such as localized neuropathic pain or inflammatory skin disorders where both pain relief and anti-inflammatory action are desired. The pump dispenser further enhances patient compliance by allowing for consistent and mess-free application.
It is important for both patients and prescribers to understand the proper use of this medication, including the appropriate dosing, application techniques, and potential side effects. As with any medication, monitoring for efficacy and adverse reactions is crucial. For any questions or concerns regarding this formulation, or to discuss its suitability for specific patient needs, please reach out to us at Bayview Pharmacy. Our team of compounding pharmacists is dedicated to providing comprehensive support and guidance to ensure optimal therapeutic outcomes.
The combination of gabapentin and mometasone furoate in a topical gel formulation is designed for targeted treatment of certain skin conditions. Gabapentin is primarily known for its use in the management of neuropathic pain, while mometasone furoate is a potent corticosteroid used for its anti-inflammatory and immunosuppressive properties. When used topically, the systemic absorption of both gabapentin and mometasone furoate is generally low; however, it is still important to consider potential drug interactions, especially in patients who are taking other medications systemically.
For gabapentin, while it does not undergo significant metabolism and does not inhibit or induce hepatic enzymes, it is excreted renally. Caution should be exercised when co-administering gabapentin with drugs that can affect renal function or compete for renal tubular secretion, such as NSAIDs, particularly in patients with renal impairment. Although the systemic absorption of topical gabapentin is minimal, patients should be monitored for signs of central nervous system (CNS) depression, such as drowsiness and dizziness, if they are concurrently taking CNS depressants like opioids, benzodiazepines, or alcohol.
Mometasone furoate, when applied topically, can interact with other corticosteroids, leading to an increased risk of systemic corticosteroid side effects, such as Cushing's syndrome and adrenal suppression, especially if used over large areas of the body, in occlusive dressings, or for prolonged periods. Patients should be advised to inform their healthcare provider if they are taking other corticosteroids or medications that can interact with corticosteroids, such as certain antifungals (e.g., ketoconazole) and HIV protease inhibitors (e.g., ritonavir), which can increase plasma levels of corticosteroids.
It is also important to consider the potential for skin irritation or contact dermatitis with any topical formulation. Patients should be instructed to report any signs of local adverse reactions, especially if they have a history of sensitivity or allergic reactions to topical products. The use of this topical gel should be done with caution in patients with a compromised skin barrier, as this could potentially increase systemic absorption of the active ingredients.
This topical gel formulation is intended for the treatment of localized neuropathic pain where an anti-inflammatory effect is also desired. It may be beneficial in conditions such as localized neurodermatitis or certain inflammatory neuropathies. However, it is not intended for widespread use or for the treatment of systemic conditions. The precise mechanism of action of gabapentin in neuropathic pain is not fully understood, but it is thought to modulate the activity of voltage-gated calcium channels. Mometasone furoate acts by reducing the release of inflammatory cytokines and other mediators.
Patients and prescribers should be aware that this is a specialized formulation and should be used under the guidance of a healthcare professional familiar with the patient's medical history and concomitant medications. If you have any questions or require further information about potential drug interactions or the suitability of this formulation for a specific patient, please reach out to us at Bayview Pharmacy for personalized advice and support.
The Gabapentin 6%/Mometasone Furoate 0.1% Topical Gel is a specialized medication formulated to deliver two active ingredients directly to the site of discomfort or inflammation on the skin. Gabapentin, originally known for its use in the management of neuropathic pain, has been found to have analgesic properties when applied topically. It works by modulating the activity of calcium channels on nerve cells, which can help to reduce the abnormal excitatory signals that contribute to pain and discomfort. This can be particularly beneficial for patients experiencing localized neuropathic pain, where the nerve fibers in the skin may be damaged or dysfunctional.
Mometasone Furoate, on the other hand, is a potent corticosteroid that exerts its effects by inducing anti-inflammatory, antipruritic, and vasoconstrictive actions. When applied to the skin, it activates natural substances in the skin to reduce swelling, redness, and itching.
The combination of Gabapentin and Mometasone Furoate in a gel base allows for the synergistic effects of both analgesic and anti-inflammatory actions. The gel formulation is designed to be easily applied through a pump mechanism, which ensures a consistent and measured dose with each use. The semisolid consistency of the gel allows it to be spread smoothly over the affected area, providing a cooling sensation upon application and ensuring that the active ingredients remain in contact with the skin for optimal absorption and effect.
This topical gel is particularly suited for patients who require targeted relief from skin conditions that involve both pain and inflammation. The precise application through the pump mechanism helps to localize treatment, minimizing systemic exposure and potential side effects that can occur with oral medications. It is important for patients and prescribers to understand that while this formulation provides localized relief, it should be used as directed to avoid overuse or potential side effects, such as skin atrophy with prolonged corticosteroid use.
For any questions regarding the use of Gabapentin 6%/Mometasone Furoate 0.1% Topical Gel, or to discuss whether this formulation is appropriate for your specific condition, please reach out to us at Bayview Pharmacy. Our team of compounding pharmacists is here to provide guidance and support to ensure appropriate treatment.
Aside from its primary indications, the Gabapentin 6%/Mometasone Furoate 0.1% Topical Gel may have a variety of other uses that can benefit patients suffering from different dermatological concerns. Gabapentin, primarily known for its role in managing neuropathic pain, when used topically, may help in the relief of localized neuropathic pain syndromes. It might offer symptomatic relief for conditions such as post-herpetic neuralgia or even complex regional pain syndrome, where abnormal skin sensations (dysesthesia) or pain are present. Moreover, gabapentin's potential anti-pruritic properties could be beneficial for reducing itch in certain dermatoses that are associated with nerve hypersensitivity or irritation.
On the other hand, Mometasone Furoate, as a medium-potency corticosteroid, plays a crucial role in reducing inflammation, itching, and redness. It may be useful in the management of other inflammatory skin diseases such as eczema, psoriasis, contact dermatitis, and discoid lupus erythematosus, provided that the conditions are limited to localized areas amenable to topical therapy.
In cosmeceutical applications, while the primary constituents are not typically aimed at cosmetic improvements, the anti-inflammatory effects of mometasone may possibly reduce skin irritation and redness associated with certain cosmetic procedures, or skin care regimes, that may provoke irritation. However, long-term use on the face or delicate skin areas should be approached with caution and under close medical supervision due to the possible side effects associated with topical steroids.
It is essential to consider that the evidence for these "other uses" is not as well established as the primary indications, and use for these conditions should be guided by a healthcare professional with an intimate understanding of the individual patient's medical history and condition. Patients or prescribers who have questions or are considering this formulation for off-label use should reach out to us at Bayview Pharmacy for more tailored information and advisement. Our team is equipped to provide comprehensive guidance to ensure appropriate treatment strategies are pursued.
Also important is the monitoring of potential side effects, such as skin atrophy or adrenal suppression with prolonged use of mometasone, or systemic side effects that might arise from significant absorption of gabapentin, although limited when administered topically. It is critical that patients report any adverse reactions or unexpected symptoms to their healthcare provider promptly.
To conclude, the Gabapentin 6%/Mometasone Furoate 0.1% Topical Gel holds potential for diverse dermatological applications beyond its primary intended use. Nevertheless, its use should be considered carefully and personalized to the patient. We at Bayview Pharmacy are here to assist with any inquiries and support healthcare professionals and patients with proper usage and optimized therapeutic outcomes.
This topical gel is typically prescribed for the treatment of various skin conditions which may include inflammatory issues or neuropathic pain. The Gabapentin component is used for nerve pain relief, while Mometasone Furoate is a potent corticosteroid that helps reduce inflammation.
Apply a thin layer of the gel to the affected area of the skin as directed by your healthcare provider. Use the pump mechanism to dispense a consistent amount of gel for each application.
It is important to use this gel only on areas recommended by your doctor. Avoid sensitive areas like the eyes, inside the mouth or nose, and the genital area unless specifically instructed by your healthcare provider.
The frequency of application will be determined by your doctor based on the condition being treated. Follow their directions carefully and do not apply more often than instructed.
Potential side effects can include skin irritation, burning, dryness, or redness at the application site. Systemic side effects are rare due to the topical nature of the formulation, but notify your healthcare provider if you encounter any unusual symptoms.
Do not cover the treated area with a bandage or wrap unless your doctor advises you to do so, as this may increase the absorption of the medication and the risk of side effects.
If you forget to apply your dose, do it as soon as you remember. If it is almost time for your next dose, skip the missed dose and resume your regular dosing schedule. Do not double the application to catch up.
Keep the gel at room temperature away from light and moisture. Do not freeze or store in the bathroom. Keep out of reach of children and pets.
Always inform your healthcare provider about any other medications or topical treatments you are using, as they may interact with this gel. It is particularly important to mention other skin products that may be drying or irritating.
The safety of this medication during pregnancy or breastfeeding has not been fully established. Please consult your healthcare provider for advice based on your specific circumstances before using this medication.
Improvement in skin condition or alleviation of pain should be evident with continued use as directed by your physician. However, if you do not notice improvement or if your symptoms worsen, contact your healthcare provider.
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.
Apply topically to affected area(s)