Mycelex - Bayer Pharmaceuticals Corp

Manufacturer
Bayer Pharmaceuticals Corp
Effective date
2006-08-14
Label type
Human prescription drug label
Version
2
Source
full-release
Hydrated at
2026-05-31 20:06:44

Label at a glance#

ProductMycelex
Label structure11 sections

Indications and uses

Mycelex ® Troches are indicated for the local treatment of oropharyngeal candidiasis.The diagnosis should be confirmed by a KOH smear and/or culture prior to treatment. Mycelex ® Troches are also indicated prophylactically to reduce the incidence of oropharyngeal candidiasis in patients immunocompromised by conditions that include chemotherapy, radiotherapy, or steroid therapy utilized in the treatment of leukemia...

Dosage and administration

Mycelex ® Troches are administered only as a lozenge that must be slowly dissolved in the mouth. The recommended dose is one troche five times a day for fourteen consecutive days. Only limited data are available on the safety and effectiveness of the clotrimazole troche after prolonged administration; therefore, therapy should be limited to short term use, if possible. For prophylaxis to reduce the incidence of or...

Label contents#

Full prescribing information#

DESCRIPTION

DESCRIPTION SECTION

Each Mycelex® Troche contains 10 mg clotrimazole [1-(o-chloro-α,α-diphenylbenzyl) imidazole], a synthetic antifungal agent, for topical use in the mouth.

Structural Formula:

DESCRIPTION
DESCRIPTION

Chemical Formula:
C22H17CIN2

The troche dosage form is a large, slowly dissolving tablet (lozenge) containing 10 mg of clotrimazole dispersed in dextrose, microcrystalline cellulose, povidone, and magnesium stearate.

CLINICAL PHARMACOLOGY

CLINICAL PHARMACOLOGY SECTION

Clotrimazole is a broad-spectrum antifungal agent that inhibits the growth of pathogenic yeasts by altering the permeability of cell membranes. The action of clotrimazole is fungistatic at concentrations of drug up to 20 mcg/mL and may be fungicidal in vitro against Candida albicans and other species of the genus Candida at higher concentrations. No single-step or multiple-step resistance to clotrimazole has developed during successive passages of Candida albicans in the laboratory; however, individual organism tolerance has been observed during successive passages in the laboratory. Such in vitro tolerance has resolved once the organism has been removed from the antifungal environment.

After oral administration of a 10 mg clotrimazole troche to healthy volunteers, concentrations sufficient to inhibit most species of Candida persist in saliva for up to three hours following the approximately 30 minutes needed for a troche to dissolve. The long term persistence of drug in saliva appears to be related to the slow release of clotrimazole from the oral mucosa to which the drug is apparently bound. Repetitive dosing at three hour intervals maintains salivary levels above the minimum inhibitory concentrations of most strains of Candida; however, the relationship between in vitro susceptibility of pathogenic fungi to clotrimazole and prophylaxis or cure of infections in humans has not been established.

In another study, the mean serum concentrations were 4.98 ± 3.7 and 3.23 ± 1.4 nanograms/mL of clotrimazole at 30 and 60 minutes, respectively, after administration as a troche.

INDICATIONS AND USAGE

INDICATIONS AND USAGE SECTION

Mycelex® Troches are indicated for the local treatment of oropharyngeal candidiasis.The diagnosis should be confirmed by a KOH smear and/or culture prior to treatment.

Mycelex® Troches are also indicated prophylactically to reduce the incidence of oropharyngeal candidiasis in patients immunocompromised by conditions that include chemotherapy, radiotherapy, or steroid therapy utilized in the treatment of leukemia, solid tumors, or renal transplantation. There are no data from adequate and well-controlled trials to establish the safety and efficacy of this product for prophylactic use in patients immunocompromised by etiologies other than those listed in the previous sentence. (See DOSAGE AND ADMINISTRATION.)

CONTRAINDICATIONS

CONTRAINDICATIONS SECTION

Mycelex® Troches are contraindicated in patients who are hypersensitive to any of its components.

WARNING

WARNINGS SECTION

Mycelex® Troches are not indicated for the treatment of systemic mycoses including systemic candidiasis.

PRECAUTIONS

PRECAUTIONS SECTION

Abnormal liver function tests have been reported in patients treated with clotrimazole troches; elevated SGOT levels were reported in about 15% of patients in the clinical trials. In most cases the elevations were minimal and it was often impossible to distinguish effects of clotrimazole from those of other therapy and the underlying disease (malignancy in most cases). Periodic assessment of hepatic function is advisable particularly in patients with pre-existing hepatic impairment.

Since patients must be instructed to allow each troche to dissolve slowly in the mouth in order to achieve maximum effect of the medication, they must be of such an age and physical and/or mental condition to comprehend such instructions.

Carcinogenesis:

CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY SECTION

An 18 month dosing study with clotrimazole in rats has not revealed any carcinogenic effect.

Usage in Pregnancy: Pregnancy Category C:

PREGNANCY

Clotrimazole has been shown to be embryotoxic in rats and mice when given in doses 100 times the adult human dose (in mg/kg), possibly secondary to maternal toxicity. The drug was not teratogenic in mice, rabbits, and rats when given in doses up to 200, 180, and 100 times the human dose.

Clotrimazole given orally to mice from nine weeks before mating through weaning at a dose 120 times the human dose was associated with impairment of mating, decreased number of viable young, and decreased survival to weaning. No effects were observed at 60 times the human dose. When the drug was given to rats during a similar time period at 50 times the human dose, there was a slight decrease in the number of pups per litter and decreased pup viability.

There are no adequate and well controlled studies in pregnant women. Clotrimazole troches should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.

PEDIATRIC USE

PEDIATRIC USE SECTION

Safety and effectiveness of clotrimazole in children below the age of 3 years have not been established; therefore, its use in such patients is not recommended.

The safety and efficacy of the prophylactic use of clotrimazole troches in children have not been established.

GERIATRIC USE

GERIATRIC USE SECTION

Clinical studies of clotrimazole did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger patients.

ADVERSE REACTIONS

ADVERSE REACTIONS SECTION

Abnormal liver function tests have been reported in patients treated with clotrimazole troches; elevated SGOT levels were reported in about 15% of patients in the clinical trials (See PRECAUTIONS section).

Nausea, vomiting, unpleasant mouth sensations and pruritus have also been reported with the use of the troche.

OVERDOSAGE

OVERDOSAGE SECTION

No data available.

DRUG ABUSE AND DEPENDENCE

DRUG ABUSE AND DEPENDENCE SECTION

No data available.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Mycelex® Troches are administered only as a lozenge that must be slowly dissolved in the mouth. The recommended dose is one troche five times a day for fourteen consecutive days. Only limited data are available on the safety and effectiveness of the clotrimazole troche after prolonged administration; therefore, therapy should be limited to short term use, if possible.

For prophylaxis to reduce the incidence of oropharyngeal candidiasis in patients immunocompromised by conditions that include chemotherapy, radiotherapy, or steroid therapy utilized in the treatment of leukemia, solid tumors, or renal transplantation, the recommended dose is one troche three times daily for the duration of chemotherapy or until steroids are reduced to maintenance levels.


HOW SUPPLIED

HOW SUPPLIED SECTION

Mycelex® Troches, white discoid, uncoated tablets are supplied in bottles of 70 and 140. Mycelex® Troches are also available for institutional use in foil packages of 70 tablets. Each tablet will be identified with the following: Mycelex 10.

Strength NDC Code Tablet
Identification
Bottles
of 70:
10 mg NDC 17314-9400-1MYCELEX 10
 
Bottles of
140:
10 mg NDC 17314-9400-3MYCELEX 10
 
Unit Dose
Package
of 70:
10 mg NDC 17314-9400-2MYCELEX 10

SPL UNCLASSIFIED SECTION

Store below 86°F (30°C).
Avoid freezing.

SPL UNCLASSIFIED SECTION

Manufactured by Bayer Pharmaceuticals Corporation
West Haven, CT 06516
Made in Germany

Distributed by Ortho-McNeil Pharmaceutical, Inc.
Raritan, NJ 08869

08753817, R.2
BAY 5097
12465
©2004 Bayer Pharmaceuticals Corporation
9/04
Printed in USA

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
309371clotrimazole 10 MG Oral LozengePSN2
206178Mycelex Troche 10 MG Oral LozengePSN2
206178clotrimazole 10 MG Oral Lozenge [Mycelex Troches]SBD2
309371clotrimazole 10 MG Oral LozengeSCD2
206178Mycelex Troches 10 MG Oral LozengeSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b64d2752-34ef-378a-1f4f-8bff32b0d1aeProduct name420250626
cb7783e0-feaa-7e56-fb3b-d43b6efa77c9Product name220250121
f31c883b-7ebf-1c60-f3b6-4ba41e8ff7a6Product name220151106
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508
f5395dd2-4395-d8c6-3477-8c2d4a2f951cProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17314-9400-1Mycelex70 in 1 BOTTLE, PLASTICTROCHE702
17314-9400-2Mycelex70 in 1 BLISTER PACKTROCHE702
17314-9400-3Mycelex140 in 1 BOTTLE, PLASTICTROCHE1402

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17314-9400MYCELEX (CLOTRIMAZOLE) TROCHE [BAYER PHARMACEUTICALS CORP]23 package rows20060918_7464e883-6286-4f04-ae38-b7ddc3fec754.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
clotrimazoleACTIVE INGREDIENTG07GZ97H652
dextroseINACTIVE INGREDIENTIY9XDZ35W22
magnesium stearateINACTIVE INGREDIENT70097M6I302
microcrystalline celluloseINACTIVE INGREDIENT2
povidoneINACTIVE INGREDIENT2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17314-940017314-9400-1, 17314-9400-3, 17314-9400-2

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 2 · 118 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
magnesium stearateMAGNESIUM STEARATE70097M6I30TABLET / SUBLINGUAL17.5 mgExact identifier — unii candidate
39 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30INSERT / VAGINAL69 mgExact identifier — unii candidate
39 equally ranked IID candidates
dextroseDEXTROSEIY9XDZ35W2SPRAY, METERED / NASAL50 mgExact identifier — unii candidate
21 equally ranked IID candidates
microcrystalline celluloseMICROCRYSTALLINE CELLULOSEOP1R32D61UGRANULE / ORAL29520 mgName fallback — name candidate
28 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30RING / VAGINAL2 mgExact identifier — unii candidate
39 equally ranked IID candidates
dextroseDEXTROSEIY9XDZ35W2INJECTION / INTRAMUSCULAR5 %w/vExact identifier — unii candidate
21 equally ranked IID candidates
povidonePOVIDONEFZ989GH94EIMPLANT / SUBCUTANEOUS6 mgName fallback — name candidate
30 equally ranked IID candidates
povidonePOVIDONEFZ989GH94ETABLET, FILM COATED, EXTENDED RELEASE / ORAL17 mgName fallback — name candidate
30 equally ranked IID candidates
microcrystalline celluloseMICROCRYSTALLINE CELLULOSEOP1R32D61UCAPSULE / ORAL2169 mgName fallback — name candidate
28 equally ranked IID candidates
dextroseDEXTROSEIY9XDZ35W2TABLET, EXTENDED RELEASE / ORAL103.95 mgExact identifier — unii candidate
21 equally ranked IID candidates
microcrystalline celluloseMICROCRYSTALLINE CELLULOSEOP1R32D61UCAPSULE, COATED PELLETS / ORAL456 mgName fallback — name candidate
28 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30GRANULE / ORAL629 mgExact identifier — unii candidate
39 equally ranked IID candidates
microcrystalline celluloseMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET, CHEWABLE / ORAL1725 mgName fallback — name candidate
28 equally ranked IID candidates
dextroseDEXTROSEIY9XDZ35W2SOLUTION / INTRAVENOUS5.05 %w/vExact identifier — unii candidate
21 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30TABLET / BUCCAL17.5 mgExact identifier — unii candidate
39 equally ranked IID candidates
povidonePOVIDONEFZ989GH94EFILM, EXTENDED RELEASE / TRANSDERMALNAName fallback — name candidate
30 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30TABLET, FOR SUSPENSION / ORAL131 mgExact identifier — unii candidate
39 equally ranked IID candidates
dextroseDEXTROSEIY9XDZ35W2TABLET / SUBLINGUAL115.78 mgExact identifier — unii candidate
21 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30POWDER / RESPIRATORY (INHALATION)0.13 mgExact identifier — unii candidate
39 equally ranked IID candidates
povidonePOVIDONEFZ989GH94ETABLET, COATED / ORAL49.2 mgName fallback — name candidate
30 equally ranked IID candidates
microcrystalline celluloseMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET, FILM COATED / ORAL992 mgName fallback — name candidate
28 equally ranked IID candidates
dextroseDEXTROSEIY9XDZ35W2TABLET, COATED / ORAL132 mgExact identifier — unii candidate
21 equally ranked IID candidates
povidonePOVIDONEFZ989GH94ECAPSULE, COATED, EXTENDED RELEASE / ORALNAName fallback — name candidate
30 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30POWDER / ORAL25 mgExact identifier — unii candidate
39 equally ranked IID candidates
povidonePOVIDONEFZ989GH94ETABLET, DELAYED RELEASE / ORAL53 mgName fallback — name candidate
30 equally ranked IID candidates
povidonePOVIDONEFZ989GH94ECAPSULE, COATED PELLETS / ORAL10.03 mgName fallback — name candidate
30 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30TABLET, DELAYED RELEASE / ORAL144 mgExact identifier — unii candidate
39 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30TABLET, EXTENDED RELEASE / ORAL173 mgExact identifier — unii candidate
39 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30TABLET, CHEWABLE / ORAL127 mgExact identifier — unii candidate
39 equally ranked IID candidates
povidonePOVIDONEFZ989GH94EDROPS / ORALNAName fallback — name candidate
30 equally ranked IID candidates
povidonePOVIDONEFZ989GH94EINJECTION / INTRAMUSCULAR0.2 %w/vName fallback — name candidate
30 equally ranked IID candidates
dextroseDEXTROSEIY9XDZ35W2CONCENTRATE / ORAL400 mgExact identifier — unii candidate
21 equally ranked IID candidates
microcrystalline celluloseMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET, FILM COATED, EXTENDED RELEASE / ORAL615 mgName fallback — name candidate
28 equally ranked IID candidates
dextroseDEXTROSEIY9XDZ35W2TABLET / ORAL183.66 mgExact identifier — unii candidate
21 equally ranked IID candidates
microcrystalline celluloseMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET, CHEWABLE, EXTENDED RELEASE / ORAL144 mgName fallback — name candidate
28 equally ranked IID candidates
microcrystalline celluloseMICROCRYSTALLINE CELLULOSEOP1R32D61USUSPENSION / ORAL1600 mgName fallback — name candidate
28 equally ranked IID candidates
povidonePOVIDONEFZ989GH94ESUSPENSION / ORAL20 mg/5mlName fallback — name candidate
30 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii candidate
39 equally ranked IID candidates
dextroseDEXTROSEIY9XDZ35W2INJECTION / INTRAVENOUS5 %w/vExact identifier — unii candidate
21 equally ranked IID candidates
microcrystalline celluloseMICROCRYSTALLINE CELLULOSEOP1R32D61UGRANULE, DELAYED RELEASE / ORAL789.6 mgName fallback — name candidate
28 equally ranked IID candidates
povidonePOVIDONEFZ989GH94ESUSPENSION/ DROPS / OPHTHALMIC0.6 %w/vName fallback — name candidate
30 equally ranked IID candidates
povidonePOVIDONEFZ989GH94ETABLET, FOR SUSPENSION / ORAL2 mgName fallback — name candidate
30 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30LOZENGE / ORAL420 mgExact identifier — unii candidate
39 equally ranked IID candidates
dextroseDEXTROSEIY9XDZ35W2SYRUP / ORAL620 mgExact identifier — unii candidate
21 equally ranked IID candidates
microcrystalline celluloseMICROCRYSTALLINE CELLULOSEOP1R32D61UPELLET / ORAL1140 mgName fallback — name candidate
28 equally ranked IID candidates
microcrystalline celluloseMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET / SUBLINGUAL43.2 mgName fallback — name candidate
28 equally ranked IID candidates
dextroseDEXTROSEIY9XDZ35W2INJECTION, SOLUTION / INTRATHECAL1925 mgExact identifier — unii candidate
21 equally ranked IID candidates
dextroseDEXTROSEIY9XDZ35W2PASTILLE / ORAL826 mgExact identifier — unii candidate
21 equally ranked IID candidates
microcrystalline celluloseMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET, ORALLY DISINTEGRATING, DELAYED RELEASE / ORAL1576 mgName fallback — name candidate
28 equally ranked IID candidates
povidonePOVIDONEFZ989GH94ETABLET / SUBLINGUAL6 mgName fallback — name candidate
30 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30IMPLANT / SUBCUTANEOUS0.5 mgExact identifier — unii candidate
39 equally ranked IID candidates
microcrystalline celluloseMICROCRYSTALLINE CELLULOSEOP1R32D61UCAPSULE, EXTENDED RELEASE / ORAL1246 mgName fallback — name candidate
28 equally ranked IID candidates
dextroseDEXTROSEIY9XDZ35W2INJECTION / INTRASPINAL75 mgExact identifier — unii candidate
21 equally ranked IID candidates
dextroseDEXTROSEIY9XDZ35W2TABLET, CHEWABLE / ORAL1286 mgExact identifier — unii candidate
21 equally ranked IID candidates
microcrystalline celluloseMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET, COATED / ORAL920 mgName fallback — name candidate
28 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30PELLET / ORAL24 mgExact identifier — unii candidate
39 equally ranked IID candidates
povidonePOVIDONEFZ989GH94ESUSPENSION / OPHTHALMIC1.8 %w/vName fallback — name candidate
30 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30WAFER / ORAL66 mgExact identifier — unii candidate
39 equally ranked IID candidates
dextroseDEXTROSEIY9XDZ35W2SOLUTION / ORAL2489 mg/5mlExact identifier — unii candidate
21 equally ranked IID candidates
povidonePOVIDONEFZ989GH94ETABLET, FILM COATED / ORAL240 mgName fallback — name candidate
30 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
045EAEE4-7E85-90BC-4EDC-499685E389F37464e883-6286-4f04-ae38-b7ddc3fec7542006-08-14Warnings, Adverse reactionsExact identifier
spl id: 045EAEE4-7E85-90BC-4EDC-499685E389F3
spl set id: 7464e883-6286-4f04-ae38-b7ddc3fec754

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.