Chloramphenicol 1% Topical Ointment is a semi-solid formulation dispensed in a tube, designed for external application to the skin. It features a greasy or oily base that facilitates the delivery of the active medication, chloramphenicol, directly to the affected area. This ointment is primarily used for the localized treatment of bacterial skin infections, aiding in reducing inflammation and promoting wound healing.

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.
Chloramphenicol 1% Topical Ointment is a compounded semi-solid formulation designed for external application to the skin. This ointment utilizes a greasy or oily base that facilitates the delivery of chloramphenicol directly to affected areas, ensuring prolonged contact with the skin for enhanced therapeutic effect. Chloramphenicol is a broad-spectrum antibiotic known for its effectiveness against a wide range of Gram-positive and Gram-negative bacteria.
By inhibiting bacterial protein synthesis, chloramphenicol slows down or stops the growth of bacteria, aiding in the resolution of the infection. The ointment should be applied as directed by your healthcare provider, typically to clean, dry skin. It is important to wash your hands before and after applying the ointment to prevent the spread of infection. Avoid contact with the eyes, mouth, and other mucous membranes unless otherwise directed.
Patients should be aware of potential side effects, which may include local skin irritation, redness, or allergic reactions. If any severe reactions occur, such as rashes, swelling, or difficulty breathing, seek medical attention immediately. Prolonged use of topical chloramphenicol should be avoided unless prescribed, as it may lead to unwanted systemic absorption and potential complications.
For prescribers, Chloramphenicol 1% Topical Ointment offers a valuable option for treating patients with bacterial skin infections, especially when other antibiotics are contraindicated or have proven ineffective. Due to its broad-spectrum activity, it can be utilized in cases where the causative organism is unknown or mixed bacterial flora are suspected. Care should be taken when prescribing to patients with a history of hypersensitivity to chloramphenicol or other components of the formulation.
Monitoring for potential systemic absorption is advisable, especially in infants, young children, or when treating large surface areas. Prescribers should educate patients on the importance of adhering to the prescribed treatment regimen and inform them about the signs of adverse reactions. Additionally, consider the potential for bone marrow suppression with chloramphenicol, although this is more commonly associated with systemic use.
If you have any questions, reach out to us.
Chloramphenicol 1% 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 formulation is typically used for conditions such as skin inflammation, infections, or wound healing.
Chloramphenicol is known to inhibit the cytochrome P450 enzyme system, particularly CYP2C19 and CYP3A4. This inhibition can lead to increased plasma concentrations of drugs metabolized by these enzymes, potentially resulting in enhanced effects or toxicity. Patients using medications such as warfarin, phenytoin, or certain antiretrovirals should be monitored closely, as chloramphenicol may increase their serum levels, necessitating dosage adjustments. Additionally, chloramphenicol may interact with other topical agents applied to the same area of the skin, potentially altering their absorption or effectiveness. It is advisable to apply other topical medications at different times or to different areas to minimize this risk.
For patients using systemic antibiotics, it is important to consider the potential for antagonistic effects. Chloramphenicol may antagonize the bactericidal activity of penicillins and cephalosporins, which could reduce the effectiveness of these antibiotics. Therefore, concurrent use should be carefully evaluated by healthcare providers, and alternative treatment options should be considered if necessary.
Patients with a history of bone marrow suppression or those currently taking medications known to cause bone marrow suppression should use chloramphenicol with caution. The systemic absorption of chloramphenicol, although minimal with topical application, could potentially exacerbate these conditions. Regular monitoring of blood counts may be warranted in such cases.
It is also important to consider the potential for allergic reactions or hypersensitivity to chloramphenicol or any of the components of the ointment base. Patients should be advised to discontinue use and seek medical attention if they experience signs of an allergic reaction, such as rash, itching, or swelling.
As with any medication, it is crucial for both patients and prescribers to be aware of these potential interactions and to communicate openly about all medications being used, including over-the-counter products and supplements. If you have any questions or concerns regarding the use of chloramphenicol 1% topical ointment, please reach out to us at Bayview Pharmacy for further guidance and support.
Chloramphenicol 1% Topical Ointment is a semi-solid formulation specifically designed for external application to the skin. This ointment is dispensed in a tube, making it convenient for precise application to affected areas. The formulation utilizes a greasy or oily base, which plays a crucial role in the delivery of the active medication, chloramphenicol, to the skin. This base not only facilitates the penetration of the medication into the skin layers but also provides a protective barrier that helps retain moisture and enhances the absorption of the therapeutic agent.
Chloramphenicol is a broad-spectrum antibiotic that works by inhibiting bacterial protein synthesis. It achieves this by binding to the 50S subunit of the bacterial ribosome, thereby preventing the growth and multiplication of bacteria. By applying the ointment directly to the skin, the medication can target the site of infection more effectively, reducing the risk of systemic side effects that might occur with oral or intravenous administration.
The greasy or oily base of the ointment not only aids in medication delivery but also provides additional therapeutic benefits. It helps to soothe and protect inflamed skin, creating an environment conducive to healing. This is particularly beneficial in conditions where the skin is compromised, such as in cases of skin inflammation, infections, or wounds. The occlusive nature of the ointment base helps to maintain skin hydration, which is essential for optimal wound healing and recovery from skin infections.
For patients, the use of Chloramphenicol 1% Topical Ointment offers a targeted approach to treating skin conditions, minimizing the potential for systemic side effects. It is important to apply the ointment as directed by a healthcare professional, ensuring that the affected area is clean and dry before application. For prescribers, this formulation provides a reliable option for managing localized skin infections and inflammation, with the added benefit of a formulation that supports skin healing and protection.
If you have any questions about Chloramphenicol 1% Topical Ointment or its use, please do not hesitate to reach out to us at Bayview Pharmacy. Our team of compounding pharmacists is here to provide you with the information and support you need to ensure the safe and appropriate use of this medication.
Chloramphenicol 1% Topical Ointment is used for treating skin conditions such as infections, inflammation, or aiding in wound healing. It is applied externally to the skin to deliver medication directly to the affected area.
Apply a thin layer of the ointment to the affected area of the skin as directed by your healthcare provider. Make sure the area is clean and dry before application. Wash your hands before and after applying the ointment.
Consult your healthcare provider before using the ointment on open wounds. While it may aid in wound healing, it is important to ensure it is appropriate for your specific condition.
Some people may experience mild side effects such as skin irritation, redness, or itching at the application site. If you experience severe reactions or symptoms persist, contact your healthcare provider.
The frequency of application will depend on your specific condition and the advice of your healthcare provider. Follow the prescribed instructions carefully.
Consult your healthcare provider before using the ointment on your face, as the skin on the face can be more sensitive. They will provide guidance based on your specific condition.
Consult a healthcare provider before using this ointment on children. They will determine if it is appropriate based on the child's age and condition.
It is best to consult your healthcare provider before using other skin products in conjunction with this ointment to avoid potential interactions or reduced effectiveness.
Store the ointment at room temperature, away from direct sunlight and moisture. Keep it out of reach of children and pets.
If you miss a dose, apply it as soon as you remember. If it is almost time for your next dose, skip the missed dose and continue with your regular schedule. Do not apply extra to make up for a missed dose.
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.
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)