cb161d23-bc41-4cec-9e42-dfeef861d161 — v2

4 Views

Version

v2

Effective date

April 17, 2007

Original packager

Sections captured

8

Identifiers

Document ID
F5990469-CB03-7E0C-6757-9DE067975C69
Set ID
cb161d23-bc41-4cec-9e42-dfeef861d161
Application numbers
Product NDCs
Package NDCs
Original packager NDCs

Names & Manufacturers

Brand names
Generic names
Manufacturer names
Product types

Substances & Pharmacology

Substance names
Routes
Pharmacologic class (PE)
Pharmacologic class (EPC)
Pharmacologic class (CS)
Mechanism of action

Other identifiers

NUI
RxCUI
UNII
UPC

Structured Label Sections

Adverse Reactions (1)

Sequence 1

Adverse Reactions: There have been isolated reports of irritation, burning, maceration, and allergic contact dermatitis associated with the application of MONISTAT-DERM.
Contraindications (1)

Sequence 1

Contraindications: MONISTAT-DERM (miconazole nitrate 2%) Cream has no known contraindications.
Description (1)

Sequence 1

Description: MONISTAT-DERM (miconazole nitrate 2%) Cream contains miconazole nitrate* 2%, formulated into a water-miscible base consisting of pegoxol 7 stearate, peglicol 5 oleate, mineral oil, benzoic acid, butylated hydroxyanisole and purified water. *Chemical name: 1-[2,4-dicholoro-B-{(2,5-dichlorobenzyl) oxy} phenethyl] imidazole mononitrate.
Dosage And Administration (1)

Sequence 1

Dosage and Administration: Sufficient MONISTAT-DERM Cream should be applied to cover affected areas twice daily (morning and evening) in patients with tinea pedis, tinea cruris, tinea corporis, and cutaneous candidiasis, and once daily in patients with tinea versicolor. If MONISTAT-DERM Cream is used in intertriginous areas, it should be applied sparingly and smoothed in well to avoid maceration effects. Early relief of symptoms (2 to 3 days) is experienced by the majority of patients and clinical improvement may be seen fairly soon after treatment is begun; however, Candida infections and tinea cruris and corporis should be treated for two weeks and tinea pedis for one month in order to reduce the possibility of recurrence. If a patient shows no clinical improvement after a month of treatment, the diagnosis should be redetermined. Patients with tinea versicolor usually exhibit clinical and mycological clearing after two weeks of treatment.
How Supplied (1)

Sequence 1

How Supplied: MONISTAT-DERM (miconazole nitrate 2%) Cream containing miconazole nitrate at 2% strength is supplied in 15g, 1 oz. and 3 oz. tubes. Ortho Dermatological Division of Ortho-McNeil Pharmaceutical, Inc. Skillman, New Jersey 08558 © OMP 2001 Printed in U.S.A. Revised February 2001 631-10-471-3
Indications And Usage (1)

Sequence 1

Indications: For topical application in the treatment of tinea pedis (athlete's foot), tinea cruris, and tinea corporis caused by Trichophyton rubrum, Trichophyton mentagrophytes, and Epidermophyton floccosum, in the treatment of cutaneous candidiasis (moniliasis), and in the treatment of tinea versicolor.
Precautions (1)

Sequence 1

Precautions: If a reaction suggesting sensitivity or chemical irritation should occur, use of the medication should be discontinued. For external use only. Avoid introduction of MONISTAT-DERM Cream into the eyes.
Spl Unclassified Section (3)

Sequence 1

MONISTAT-DERM Miconazole nitrate Miconazole Miconazole nitrate Pegoxol 7 stearate Peglicol 5 oleate Mineral oil Benzioc acid Butylated hydroxyanisole Water

Sequence 2

For Topical Use Only

Sequence 3

Actions: Miconazole nitrate is a synthetic antifungal agent which inhibits the growth of the common dermatophytes, Trichophyton rubrum, Trichophyton mentagrophytes, and Epidermophyton floccosum, the yeast-like fungus, Candida albicans, and the organism responsible for tinea versicolor (Malassezia furfur).