Nitrofurazone 0.2% Topical Ointment is a semi-solid formulation dispensed in a tube for external application to the skin. It provides a greasy or oily base that aids in the delivery of medication for localized treatment. This prescription medication is typically used for treating conditions such as Impetigo, Folliculitis, Cellulitis, Erysipelas, and Furunculosis, promoting skin inflammation reduction, infection control, and wound healing.

Licensed to fill prescriptions for patients in RI, MA, CT, NJ, NH, FL and ME. New York patients are served on a limited basis while nonresident registration is pending.
Nitrofurazone 0.2% Topical Ointment is a prescription medication specifically designed to treat a variety of skin conditions.
This semi-solid formulation is dispensed in a tube and is intended for external application to the skin. The ointment provides a greasy or oily base that aids in the delivery of the medication. It is typically used for conditions such as skin inflammation, infections, or wound healing. However, it is important to note that Nitrofurazone 0.2% Topical Ointment is not suitable for treating viral skin infections such as cold sores, chickenpox, or shingles.
Generally, Nitrofurazone 0.2% Topical Ointment is well tolerated by most patients. The most common side effects include mild skin irritation and a burning sensation. It is crucial to follow the directions on the prescription label and to use the medication for the full course of treatment to ensure its effectiveness. If you have any questions or concerns about Nitrofurazone 0.2% Topical Ointment, please do not hesitate to reach out for further information.
This Nitrofurazone 0.2% Topical Ointment is a semi-solid formulation designed for external application to the skin. It is dispensed in a tube and provides a greasy or oily base that aids in the delivery of the medication for localized treatment. It is typically used for conditions such as skin inflammation, infections, or wound healing.
The ointment is indicated for the treatment of superficial skin infections caused by susceptible bacteria, such as furunculosis, impetigo, and secondary bacterial infections of burns and wounds. It is also used for the prevention of infection in minor cuts, scrapes, and burns.
Patients should avoid contact with the eyes, nose, and mouth while using this ointment. If contact occurs, the area should be rinsed thoroughly with water. It is also advised to avoid contact with other mucous membranes, such as the vagina or rectum, as this may cause irritation.
It is important to use this ointment for the full course of treatment, even if symptoms improve after a few days. If symptoms worsen or do not improve after 7 days of treatment, patients should contact their healthcare provider.
Patients should avoid using other topical medications while using this ointment, as this may increase the risk of adverse reactions. It is also advised to avoid using this ointment on large areas of skin or for prolonged periods of time, as this may increase the risk of systemic absorption and adverse reactions.
Pregnant or breastfeeding patients should avoid using this ointment, as it may be absorbed systemically and cause harm to the fetus or infant. Patients should inform their healthcare provider of any other medications they are taking, as this may increase the risk of interactions.
If you have any questions about this formulation or its use, please reach out to your healthcare provider.
Nitrofurazone 0.2% Topical Ointment is a semi-solid formulation, dispensed in a tube, designed for external application to the skin. This medication is primarily used to treat a variety of skin conditions, including bacterial and fungal infections. It functions by eliminating the bacteria or fungi causing the infection, providing localized treatment directly to the affected area.
Typically, Nitrofurazone 0.2% Topical Ointment is applied two to three times a day, or as directed by your healthcare provider. Prior to application, it is crucial to cleanse the affected area with soap and water to remove any potential dirt or debris. Once the area is thoroughly dried, a thin layer of the ointment should be gently rubbed into the skin.
Unless otherwise instructed by your healthcare provider, it is generally not recommended to cover the treated area with a bandage or other dressing. This allows the skin to breathe and aids in the healing process. It is also important to continue using Nitrofurazone 0.2% Topical Ointment for the full course of treatment prescribed by your doctor, even if symptoms improve before the completion of the treatment course. Discontinuing the medication prematurely may result in the return of the infection.
If you have any questions or concerns regarding the use of Nitrofurazone 0.2% Topical Ointment, do not hesitate to seek advice from your healthcare provider. They can provide you with the most accurate and personalized information based on your specific condition and treatment needs.
Nitrofurazone 0.2% Topical Ointment is a semi-solid formulation designed for external application to the skin. It is dispensed in a tube and provides a greasy or oily base that aids in the delivery of the medication for localized treatment. This ointment is typically used for conditions such as skin inflammation, infections, or wound healing. It is also beneficial in treating superficial skin infections caused by bacteria, skin ulcers, and skin infections caused by fungi. Furthermore, it can be used to treat skin infections caused by parasites, such as scabies.
The Nitrofurazone 0.2% Topical Ointment should be applied to the affected area two to three times daily, or as directed by a healthcare provider. It is important to note that this formulation should not be used for more than two weeks, and should not be used on large areas of the body. If you have any questions about the use of this formulation, please consult with a healthcare provider. This ointment is a powerful tool in the treatment of various skin conditions and infections, providing relief and promoting healing.
Nitrofurazone 0.2% Topical Ointment is a semi-solid formulation designed for external application to the skin. It is dispensed in a tube and provides a greasy or oily base that aids in the delivery of medication or therapeutic agents for localized treatment.
This ointment is typically used for conditions such as skin inflammation, infections, or wound healing. It helps to treat and prevent bacterial infections on the skin.
Apply a thin layer of the ointment to the affected area as directed by your healthcare provider. The ointment should be gently rubbed into the skin until it is fully absorbed.
Yes, Nitrofurazone 0.2% Topical Ointment can be used on open wounds. It aids in wound healing by preventing bacterial infections.
Generally, it is safe for all skin types. However, if you have sensitive skin or known allergies, it is recommended to consult with your healthcare provider before using this ointment.
No, Nitrofurazone 0.2% Topical Ointment is not designed to treat fungal infections. It is primarily used for bacterial skin infections and inflammation.
If you experience any side effects such as skin irritation, redness, or swelling, stop using the ointment and contact your healthcare provider immediately.
It is generally safe to use on the face, but avoid contact with the eyes. If the ointment gets into your eyes, rinse thoroughly with water and contact your healthcare provider.
The frequency of application depends on the severity of your condition. Your healthcare provider will provide specific instructions based on your individual needs.
If you are pregnant or breastfeeding, consult with your healthcare provider before using this ointment. The effects of this medication on an unborn baby or nursing infant are not fully known.
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, NJ, NH, FL, and ME; 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)