Prescription medication · Topical Corticosteroid
mometasone topical
Also sold as Elocon. This cream treats skin problems that cause swelling, redness, and itching.
Data updated 2026-05-15
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mometasone topical (Elocon) is a prescription Topical Corticosteroid. This cream treats skin problems that cause swelling, redness, and itching.
Mometasone Furoate Cream is a medicine that reduces skin inflammation and itching. It belongs to a class of drugs called topical corticosteroids.
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What it does
This cream treats skin problems that cause swelling, redness, and itching.
Common side effects
Burning, Itching, Skin thinning
Key warnings
Using too much mometasone cream or using it for a long time can affect your hormone levels.
The sections below are summarized in plain English from mometasone topical's FDA-approved prescribing information. They describe what the official label says, and are not personal medical advice.
How It Works
Mometasone Furoate Cream works by reducing inflammation in the skin. It does this by blocking certain substances in the body that cause swelling and itching. This helps to relieve the symptoms of skin conditions.
How to Take It
Apply a thin layer of the cream to the affected skin once a day. Only use it on the areas that need treatment. Stop using the cream when your skin gets better. If your skin does not improve after 2 weeks, talk to your doctor.
This is a plain-language summary of mometasone topical's FDA labeling, not individualized dosing advice. Ask a pharmacist or prescriber before changing how you take this medication.
Pregnancy & Breastfeeding
If you are pregnant, only use this cream if your doctor says it is okay. It is not known if this medicine passes into breast milk. Talk to your doctor before using it if you are breastfeeding.
This is a plain-language summary of mometasone topical's FDA labeling, not individualized advice. Ask a pharmacist or prescriber about pregnancy or breastfeeding on this medication.
Missed Dose
Apply the missed dose as soon as you remember. If it is almost time for your next dose, skip the missed dose and continue with your regular schedule.
This is a plain-language summary of mometasone topical's FDA labeling, not individualized advice. Ask a pharmacist or prescriber what to do about your specific missed dose.
Storage
Store the cream at room temperature, away from excessive heat.
Serious Warnings
Using too much mometasone cream or using it for a long time can affect your hormone levels. This can cause problems like Cushing's syndrome or high blood sugar. Children are more likely to get these side effects. This medicine may also increase your risk of cataracts and glaucoma. Tell your doctor if you have blurred vision.
Known Drug Interactions
7 DRUG INTERACTIONS No drug-drug interaction studies have been conducted with mometasone furoate cream.
Mechanism: There have been no specific studies done to see how these two forms of the same medicine interact with each other.
What to do: Consult your doctor or pharmacist before using multiple products with the same active ingredient to prevent using too much.
This is a plain-language summary of interactions documented in FDA labeling, not individualized advice. Ask a pharmacist or prescriber before combining medications.
Common Questions
Can I use this cream on my face?
Can I cover the treated area with a bandage?
What should I do if the cream gets in my eyes?
Can children use this cream?
How long should I use this cream?
What are the signs of skin thinning?
Can this cream cause allergic reactions?
Is it safe to use this cream with other medications?
What should I do if I experience burning or itching?
Can this cream cause vision problems?
What are the common side effects of mometasone topical?
Does mometasone topical interact with other medications?
What drug class is mometasone topical?
Is mometasone topical safe during pregnancy?
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What the FDA Data Shows for mometasone topical
The FDA label for mometasone topical (sold under brand names such as Elocon) classifies it as a prescription-only medication in the Topical Corticosteroid class. This cream treats skin problems that cause swelling, redness, and itching. Official labeling lists 3 commonly reported side effects, including Burning, Itching, Skin thinning.
Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. Voluntary reports accumulate over the lifetime of a drug and reflect wide-ranging clinical use. The database also lists 1 documented drug interaction derived from FDA labeling, with the top-flagged interaction rated minor severity. Acquisition-cost data is surveyed weekly by CMS and updated as manufacturers report changes.
Report counts do not establish causation, a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history, and patent information further shape supply and switching decisions. This page summarizes public FDA data for educational purposes only and is not a substitute for professional medical advice, always consult a licensed healthcare provider before starting, stopping, or changing any medication.
Data Sources
Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS).
FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. Always consult a healthcare professional before making medication decisions.
Last updated: July 9, 2019
Read our methodology - how this data is sourced, computed, and verified.
Data currency: FDA FAERS adverse-event reports through 2025, CMS NADAC acquisition-cost pricing effective December 2024, compiled and last refreshed May 2026. See our methodology for per-source dates and refresh cadence. Spot a figure that looks wrong? Report a correction.
All federal data sources used on this page
- FDA Orange Book - approved drug products with therapeutic equivalence. accessdata.fda.gov/cder/ob
- FDA DailyMed - NIH-hosted drug labeling for FDA-approved meds. dailymed.nlm.nih.gov
- FDA Adverse Event Reporting System (FAERS) - post-marketing safety surveillance. fda.gov/drugs/faers
- NLM RxNorm - standardized clinical drug nomenclature. nlm.nih.gov/research/umls/rxnorm
- CMS Medicare Part B Drug Average Sales Price Files - federal drug pricing data. cms.gov/medicare/part-b-drugs/asp
- FDA Drug Shortages Database - current and resolved drug shortage tracking. accessdata.fda.gov/drugshortages