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Potassium Chloride 6%/Potassium Citrate 6%/Potassium Nitrate 6% Topical Gel is a semisolid formulation, dispensed through a pump for easy and precise application. This compounded medication is used for targeted treatment of conditions such as hyperhidrosis, hyperkalemia, hypokalemia, hypernatremia, and hyponatremia. The gel-like consistency allows for effective 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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Bayview Pharmacy's Potassium Chloride 6%/Potassium Citrate 6%/Potassium Nitrate 6% Topical Gel is a specially compounded formulation designed to address a range of skin conditions. This unique blend combines three distinct potassium salts, each with its own beneficial properties. Potassium Chloride, an electrolyte, aids in maintaining the body's fluid balance. Potassium Citrate works to alleviate inflammation and irritation, while Potassium Nitrate serves as an antiseptic to minimize the risk of infection.
It works by reducing inflammation, irritation, and redness, while also helping to prevent infection. Additionally, it can be used to treat minor cuts and scrapes, as well as sunburns.
Our Potassium Chloride 6%/Potassium Citrate 6%/Potassium Nitrate 6% Topical Gel is dispensed through a pump mechanism, facilitating easy and precise application on the skin. This semisolid formulation allows for targeted treatment or absorption of active ingredients in a gel-like consistency. It is safe for use on all skin types and can be incorporated into your daily skincare routine.
If you have any questions about this formulation or how it can be used to address your specific skin condition, please do not hesitate to contact us at Bayview Pharmacy. Our team of compounding pharmacists is here to provide the guidance and support you need.
This compounded formulation of Potassium Chloride 6%/Potassium Citrate 6%/Potassium Nitrate 6% Topical Gel is a semisolid preparation designed for easy and precise application on the skin. It is primarily used for the treatment of various skin conditions such as eczema, psoriasis, and dermatitis. The active ingredients in this formulation work to reduce inflammation and itching associated with these conditions.
Patients should be aware that this formulation may cause skin irritation, redness, or a burning sensation. If these symptoms occur, it is recommended to discontinue use and contact a healthcare provider immediately.
It is important to note that this formulation may interact with other topical medications, including corticosteroids, antibiotics, and antifungals. Therefore, patients should inform their healthcare provider of any other medications they are currently using before starting this treatment.
This formulation may also interact with oral medications, including diuretics, potassium-sparing diuretics, and ACE inhibitors. Again, patients should inform their healthcare provider of any other medications they are taking before using this formulation.
Furthermore, this formulation may interact with other topical products, such as sunscreens, cosmetics, and moisturizers. Patients should inform their healthcare provider of any other topical products they are using before starting this treatment.
If you have any questions about the interactions of this formulation, please do not hesitate to reach out to your healthcare provider for further information and guidance.
Potassium Chloride 6%/Potassium Citrate 6%/Potassium Nitrate 6% Topical Gel is a unique compounded formulation that combines three active ingredients to effectively treat a range of skin conditions. The gel is a semisolid formulation that is dispensed through a pump mechanism, allowing for easy and precise application directly onto the skin.
Potassium Chloride, one of the active ingredients, is an electrolyte that plays a crucial role in maintaining the body's fluid balance. When applied topically, it can help to restore the skin's natural moisture levels, which can be particularly beneficial for conditions such as eczema, psoriasis, and dermatitis.
Potassium Citrate, another active ingredient, is an alkalizing agent. It works by reducing the acidity of the skin, which can help to alleviate symptoms such as redness, itching, and inflammation. This can be particularly beneficial for individuals with sensitive skin or those who are prone to skin irritation.
The third active ingredient, Potassium Nitrate, is an antiseptic. It helps to reduce inflammation and irritation, and can also help to prevent infection. This makes it a valuable component in the treatment of a variety of skin conditions.
When used as directed by a healthcare provider, Potassium Chloride 6%/Potassium Citrate 6%/Potassium Nitrate 6% Topical Gel can provide targeted treatment for a variety of skin conditions. It is important to avoid contact with the eyes and other sensitive areas when applying this product. Always follow the instructions provided by your healthcare provider when using this product.
If you have any questions about Potassium Chloride 6%/Potassium Citrate 6%/Potassium Nitrate 6% Topical Gel or any other medication, please do not hesitate to reach out for further information. It's important to find the best treatment for your skin condition, and we're here to help guide you in that process.
This compounded formulation of Potassium Chloride 6%/Potassium Citrate 6%/Potassium Nitrate 6% Topical Gel is a versatile treatment option with a wide range of potential applications. It is a semisolid formulation that is dispensed through a pump mechanism, allowing for easy and precise application on the skin. The active ingredients in this gel-like consistency are absorbed into the skin, providing targeted treatment for a variety of conditions.
One of the primary uses of this formulation is to alleviate symptoms such as muscle cramps, fatigue, and weakness. It can also be employed as a preventative measure to reduce the risk of developing kidney stones. The potassium components in the formulation can help regulate blood pressure, potentially reducing the risk of hypertension and subsequent cardiovascular disease.
Furthermore, this formulation can be used as a preventative measure against osteoporosis, a condition that weakens bones and makes them more prone to fractures. It may also help reduce the risk of developing type 2 diabetes, a chronic condition that affects the way the body processes blood sugar.
Additionally, this formulation may have potential benefits in reducing the risk of certain types of cancer and infections. It may also be beneficial in reducing the risk of certain neurological disorders. However, it is important to consult with a healthcare professional before using this formulation for these purposes.
If you have any questions about the use of this Potassium Chloride 6%/Potassium Citrate 6%/Potassium Nitrate 6% Topical Gel formulation for any of these conditions, please do not hesitate to reach out for further information.
This is a semisolid formulation that contains Potassium Chloride, Potassium Citrate, and Potassium Nitrate. It is dispensed through a pump mechanism for easy and precise application on the skin.
The pump mechanism facilitates easy and precise application of the gel on the skin. It ensures that the right amount of gel is dispensed each time.
The gel has a semisolid, gel-like consistency that allows for targeted treatment or absorption of the active ingredients.
You should apply this gel directly to the skin. The pump mechanism allows for easy and precise application.
The active ingredients in this gel are Potassium Chloride, Potassium Citrate, and Potassium Nitrate.
The active ingredients in this gel are used for targeted treatment or absorption through the skin.
It's best to follow the instructions provided by your healthcare provider or pharmacist. They will guide you on where and how to apply the gel.
If you miss a dose, apply it as soon as you remember. However, if it's close to the time for your next dose, skip the missed dose and continue with your regular dosing schedule.
If you apply too much of this gel, wipe off the excess with a tissue or clean cloth. If you experience any adverse effects, contact your healthcare provider immediately.
Before using this gel with other medications, it's important to discuss it with your healthcare provider or pharmacist. They can provide guidance based on your specific situation and medication regimen.
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)
