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Eczemol

Generic: Potassium Bromide, Nickel Sulfate, and Sulfur

Verified·Apr 23, 2026
Manufacturer
Shalina Healthcare
NDC
61480-127
Route
ORAL
ICD-10 indication
L20.9

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About Eczemol

Eczemol is a triple-action topical cream containing Clobetasol Propionate (corticosteroid), Neomycin Sulphate (antibiotic), and Miconazole Nitrate (antifungal). It is indicated for the treatment of inflammatory skin conditions such as eczema and dermatitis, particularly when complicated by secondary bacterial or fungal infections.

Copay & patient assistance

Detailed copay and financial assistance information is not publicly available for this medication at this time. Please consult your pharmacist or the manufacturer's official patient support program for more details.

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Prescribing information

From the FDA-approved label for Eczemol. Official source: DailyMed (NLM) · Label effective Nov 20, 2025

Indications and usage
INDICATIONS ECZEMOL ® is indicated for the treatment of moderate to severe eczema and atopic dermatitis. It has been found to work well with a variety of combination therapies.
Dosage and administration
DOSAGE AND ADMINISTRATION Absorption of nickel sulphate is variable among individuals. For maximum absorption, tablets should be taken orally at the beginning of the day (or any convenient time after having taken nothing but water for at least 7 hours). Take nothing but water for one hour after taking medication to aid absorption. Kg lbs Starting dose Max Daily dose 5-11 11-25 ¼ ½ 12-22 26-50 ½ 1 23-45 51-100 1 2 46-68 101-150 2 4 69-90 151-200 3 6 91+ 201+ 4 8 In the setting of renal impairment Dosage should be adjusted and serum nickel and bromide levels should be followed. Steady state trough level should be drawn prior to ingesting the day's dose after one week of dosing or at appropriate intervals. Target trough serum nickel level is 20-40 mcg/L. (Caution: post dose peak levels are unreliable.) Treatment duration depends on the individual. Increase dose as needed on a monthly basis. Try b.i.d. dosing (upon rising and at bedtime) if max dose (see above ) is not effective; do not exceed max daily dose. Maintenance phase In order to maintain symptomatic relief, medication may be continued at the same or reduced initial phase dose level.
Contraindications
CONTRAINDICATIONS Although there are no known contraindications, patients who are allergic to any ECZEMOL ® ingredient should consult a physician prior to taking the medication. (Refer to Section on Hypersensitivity)
Warnings
WARNING Do not use if imprinted seal under bottle cap is missing or broken. Do not use if pregnant or nursing. If allergic to nickel or metal objects such as jewelry or if there is a history of blistering hand eczema, see PRECAUTIONS for hypersensitivity information. Lactose intolerant patients may have gastrointestinal difficulty. This has very rarely been reported at the doses used.
Drug interactions
Drug interactions There are no known drug interactions.
Adverse reactions
ADVERSE REACTIONS ECZEMOL ® contains low doses of active ingredients. Therefore there are minimal known side effects. (see PRECAUTIONS for hypersensitivity information)
Use in pregnancy
Pregnancy Pregnancy category C Animal reproduction studies have not been conducted with ECZEMOL ® . ECZEMOL ® should not be given to a pregnant woman.

Label text is reproduced as-is from the FDA-approved label. We do not paraphrase, summarize, or omit. Content above is for informational purposes only and is not medical advice. Always consult your prescribing clinician or pharmacist before making decisions about your medication.

Conditions we've indexed resources for

Click a condition to see copay cards, grants, and PA rules specific to it. For the full list of FDA-approved indications, see Prescribing information above.

Prior authorization & coverage

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How this page is sourced

  • Drug identity verified against openFDA NDC Directory.
  • Label text (when shown) originates from NLM DailyMed.
  • Copay and assistance URLs verified periodically; if you hit a broken link, tell us.