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Diclofenac Sodium 5%/Lidocaine 2%/Prilocaine 2% Topical Gel is a semisolid formulation dispensed through a pump mechanism. This combination medication is designed for easy and precise application on the skin, providing targeted treatment for conditions such as osteoarthritis, rheumatoid arthritis, tendinitis, bursitis, and neuropathic pain. The gel-like consistency ensures optimal absorption of the active ingredients.
Licensed to fill prescriptions for patients in RI, MA, CT, NY, NJ, NH, FL and ME.
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This compounded formulation of Diclofenac Sodium 5%/Lidocaine 2%/Prilocaine 2% Topical Gel is a semisolid preparation that is dispensed through a pump mechanism. This design allows for easy and precise application on the skin, targeting the specific area for treatment or absorption of the active ingredients. The gel-like consistency ensures a smooth application process, enhancing the user's experience.
The formulation is a potent treatment for a variety of musculoskeletal conditions, including osteoarthritis, rheumatoid arthritis, tendinitis, bursitis, and neuropathic pain. The combination of Diclofenac Sodium, Lidocaine, and Prilocaine provides a powerful analgesic effect, reducing inflammation and pain. Diclofenac Sodium is a non-steroidal anti-inflammatory drug (NSAID) that works by blocking the production of certain chemicals in the body that cause inflammation and pain. Lidocaine and Prilocaine, on the other hand, are local anesthetics that work by blocking nerve signals in the affected area, providing immediate relief from pain.
It is generally well-tolerated, with few side effects. However, it is crucial to follow the instructions provided by your healthcare provider and to use the medication as directed. If you have any questions about this formulation or how to use it, please reach out to your healthcare provider or pharmacist.
This compounded formulation of Diclofenac Sodium 5%/Lidocaine 2%/Prilocaine 2% Topical Gel is a semisolid preparation designed for easy and precise application on the skin. It is dispensed through a pump mechanism, ensuring targeted treatment or absorption of the active ingredients in a gel-like consistency. This formulation is primarily used for the treatment of conditions such as Osteoarthritis, Rheumatoid Arthritis, Tendinitis, Bursitis, and Neuropathic Pain.
The mechanism of action is believed to be through the reduction of inflammation and provision of local anesthetic relief. It is crucial to remember that this formulation should not be applied to open wounds or areas of skin that are broken or irritated. Always follow the directions provided by your healthcare provider when using this formulation. Typically, a thin layer of the gel is applied to the affected area and gently massaged into the skin. Remember to wash your hands after applying the gel.
Patients should be aware that this formulation may cause skin irritation, redness, or burning. If these side effects occur, discontinue use and contact your healthcare provider immediately. This formulation may also interact with other medications, including non-steroidal anti-inflammatory drugs (NSAIDs), anticoagulants, and anticonvulsants. Therefore, it is essential to inform your healthcare provider of any other medications you are taking before starting this treatment.
This formulation is not recommended for use in children under the age of 12. If you have any questions or concerns about this formulation or its use, please do not hesitate to reach out to your healthcare provider for further information and guidance.
This compounded formulation of Diclofenac Sodium 5%/Lidocaine 2%/Prilocaine 2% Topical Gel is a semisolid preparation designed for easy and precise application on the skin. The gel is dispensed through a pump mechanism, ensuring targeted treatment or absorption of the active ingredients. The formulation combines three active ingredients: Diclofenac Sodium 5%, Lidocaine 2%, and Prilocaine 2%, each serving a specific purpose in the treatment of various musculoskeletal conditions.
Diclofenac Sodium, a nonsteroidal anti-inflammatory drug (NSAID), works by reducing inflammation and pain associated with conditions such as osteoarthritis, rheumatoid arthritis, tendinitis, and bursitis. Lidocaine and Prilocaine, on the other hand, are local anesthetics that numb the skin and surrounding area, providing relief from neuropathic pain.
The gel is applied directly to the affected area, facilitating the absorption of the active ingredients into the skin. It can be used up to four times a day, depending on the severity of the condition and the advice of your healthcare provider. However, it is crucial to avoid applying the gel on open wounds, broken, or irritated skin to prevent adverse reactions. Similarly, avoid contact with the eyes, nose, and mouth. In case of accidental contact, rinse the area thoroughly with water.
It is always recommended to follow the instructions provided by your healthcare provider or pharmacist when using this formulation. If you have any questions or concerns about the use of this topical gel, do not hesitate to seek professional advice.
This compounded formulation of Diclofenac Sodium 5%/Lidocaine 2%/Prilocaine 2% Topical Gel is a versatile treatment option for a variety of musculoskeletal conditions, including muscle strains, sprains, and contusions. Chronic pain conditions such as fibromyalgia and complex regional pain syndrome can also be alleviated with this formulation.
Furthermore, this topical gel formulation can be used to treat neuropathic pain associated with diabetic neuropathy, post-herpetic neuralgia, and trigeminal neuralgia. It is also beneficial in managing pain associated with cancer and its treatments. This formulation can be used in conjunction with other medications to enhance pain relief.
Generally well-tolerated, this topical gel formulation should not be applied on open wounds or on areas of skin that are broken or irritated. It is also not suitable for application on the face, eyes, or mucous membranes. Patients are advised to avoid contact with the eyes and to wash their hands thoroughly after application.
If you have any queries regarding the use of this formulation for other conditions, please do not hesitate to contact us. We are here to assist you with your healthcare needs.
This is a semisolid formulation that contains Diclofenac Sodium, Lidocaine, and Prilocaine. It is dispensed through a pump mechanism for easy and precise application on the skin.
The gel has a semisolid, gel-like consistency that allows for targeted treatment or absorption of the active ingredients.
The gel is applied topically on the skin. It is dispensed through a pump mechanism, which facilitates easy and precise application.
The pump mechanism allows for easy and precise application of the gel on the skin. This ensures that the right amount of gel is applied to the targeted area.
The active ingredients in this topical gel are Diclofenac Sodium, Lidocaine, and Prilocaine.
Diclofenac Sodium is a nonsteroidal anti-inflammatory drug (NSAID) that helps to reduce pain, inflammation, and swelling.
Lidocaine and Prilocaine are local anesthetics that work by causing temporary numbness/loss of feeling in the skin and surrounding tissues.
This gel is typically used for targeted treatment of specific areas of the body. It's best to consult with a healthcare provider to determine if this gel is suitable for your specific type of pain.
The frequency of application can vary depending on the individual's condition and the healthcare provider's recommendation. Always follow the instructions provided by your healthcare provider or pharmacist.
As with any medication, there can be potential side effects. These can include skin irritation or sensitivity at the application site. If you experience any unusual symptoms, it's important to contact your healthcare provider immediately.
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.
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.
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, NY, NJ, NH, FL, and ME. 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)
