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Mometasone Topical (Asmanex): Uses, Side Effects and Dosage

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Facts
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Prescription (Rx)
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1 mg/g
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Patient information: uses, side effects, how to take - Mometasone Topical

What is mometasone furoate cream, USP, 0.1%?

  • Mometasone furoate cream, USP, 0.1% is a prescription medicine used on the skin (topical) for the relief of redness, swelling, heat, pain (inflammation) and itching, caused by certain skin problems in people 2 years of age and older.
  • It is not known if mometasone furoate cream, USP, 0.1% is safe and effective for use in children under 2 years of age.

  • Mometasone furoate cream, USP, 0.1% should not be used in children under 2 years of age.
  • It is not known if mometasone furoate cream, USP, 0.1% is safe and effective for use in children longer than 3 weeks.

Do not use mometasone furoate cream, USP, 0.1% if youare allergic to mometasone furoate or any of the ingredients in mometasone furoate cream, USP, 0.1%. See the end of this leaflet for a complete list of ingredients in mometasone furoate cream, USP, 0.1%.

Before using mometasone furoate cream, USP, 0.1%, tell your healthcare provider about all your medical conditions, including if you:

  • have a skin infection at the site to be treated. You may also need medicine to treat the skin infection.
  • are pregnant or plan to become pregnant. It is not known if mometasone furoate cream, USP, 0.1% will harm your unborn baby.

  • are breastfeeding or plan to breastfeed. It is not known if mometasone furoate cream, USP, 0.1% passes into your breast milk. Tell your healthcare provider about all the medicines you take,including prescription and over-the-counter medicines, vitamins, and herbal supplements.

Especially tell your healthcare provider if you take other corticosteroid medicines by mouth or use other products on your skin or scalp that contain corticosteroids.

How should I use mometasone furoate cream, USP, 0.1%?• Use mometasone furoate cream, USP, 0.1% exactly as your healthcare provider tells you to use it.

  • Apply a thin film of mometasone furoate cream, USP, 0.1% to the affected skin area 1 time each day.
  • Tell your healthcare provider if the treated skin area does not get better after 2 weeks of treatment.
  • Do not bandage, cover, or wrap the treated skin area unless your healthcare provider tells you to.
  • Mometasone furoate cream, USP, 0.1% should not be used to treat diaper rash or redness. Do not apply mometasone furoate cream, USP, 0.1% in the diaper area if wearing diapers or plastic pants.
  • Avoid using mometasone furoate cream, USP, 0.1% on the face, groin, or underarms (armpits).
  • Wash your hands after applying mometasone furoate cream, USP, 0.1%.

What are the possible side effects of mometasone furoate cream, USP, 0.1%?

Mometasone furoate cream, USP, 0.1% may cause serious side effects, including:

  • Mometasone furoate cream, USP, 0.1% can pass through your skin.

Too much mometasone furoate cream, USP, 0.1% passing through your skin can cause your adrenal glands to stop working properly. Your healthcare provider may do blood tests to check for adrenal gland problems.

  • Vision problems.Topical corticosteroids may increase your chance of developing vision problems such as cataract and glaucoma. Tell your healthcare provider if you develop blurred vision or other vision problems during treatment with mometasone furoate cream, USP, 0.1%.
  • Skin problems.Skin problems may happen during treatment with mometasone furoate cream, USP, 0.1%, including allergic reactions (contact dermatitis) and skin infections at the treatment site. Stop using mometasone furoate cream, USP, 0.1% and tell your healthcare provider if you develop any skin reactions such as pain, tenderness, swelling, or problems healing during treatment with mometasone furoate cream, USP, 0.1%.

The most common side effects of mometasone furoate cream, USP, 0.1% includeburning, itching, and thinning of the skin (atrophy). These are not all the possible side effects of mometasone furoate cream, USP, 0.1%. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

How should I store mometasone furoate cream, USP, 0.1%?• Store mometasone furoate cream, USP, 0.1% at 25°C (77°F); excursions permitted to 15-30°C (59-86°F) [see USP Controlled Room Temperature]. Avoid excessive heat.

  • Keep mometasone furoate cream, USP, 0.1% and all medicines out of the reach of children.

General information about the safe and effective use of mometasone furoate cream, USP, 0.1%.Medicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet. Do not use mometasone furoate cream, USP, 0.1% for a condition for which it was not prescribed. Do not give mometasone furoate cream, USP, 0.1% to other people, even if they have the same symptoms that you have. It may harm them. You can ask your pharmacist or healthcare provider for information about mometasone furoate cream, USP, 0.1% that is written for health professionals.

What are the ingredients in mometasone furoate cream, USP, 0.1%?

Active ingredient:mometasone furoate

Inactive ingredients:hexylene glycol, phosphoric acid, propylene glycol stearate, stearyl alcohol and ceteareth-20, titanium dioxide, aluminum starch ocetnylsuccinate, white wax, white petrolatum, and purified water.

Distributed by:

Cosette Pharmaceuticals, Inc.

South Plainfield, NJ 07080

8-0634CPLNC2 Revised: 03/2022 VC7619

This Patient Information has been approved by the U.S. Food and Drug Administration.

About this document

Source: FDA drug labeling via NLM DailyMed · Application number: ANDA 077447 · View the label on DailyMed

Revision date stated in the text: March 2022

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The information on this site does not replace the advice of a doctor or pharmacist.

Drug information for Mometasone Topical

Rx or OTC
Prescription (Rx)?
  • This drug is available only with a prescription from a licensed healthcare provider.
  • Rx
Drug class Corticosteroid
Active ingredient Mometasone furoate 1 mg/g
Dosage form Cream
Route Topical
Marketing status listed in the FDA NDC Directory
Company (applicant) COSETTE PHARMS NC
FDA approval ANDA 077447Abbreviated New Drug Application (ANDA) – generic drug Approved May 22, 2006
Therapeutic equivalence (TE) code ABCodes starting with A mean the FDA rates the drug therapeutically equivalent to its reference drug (Orange Book).
Manufacturers 5 labelers list this drug on DailyMed
Packages (NDC)
Package
1 mg/g – 15 g in 1 tube / 1 in 1 carton NDC 0713-0634-15
1 mg/g – 45 g in 1 tube / 1 in 1 carton NDC 0713-0634-37

Source: FDA drug labeling via NLM DailyMed, data as of November 2, 2026. FDA data (DailyMed, Orange Book, Drug Shortages, enforcement reports). Not a substitute for the advice of a doctor or pharmacist.