Your browser does not support JavaScript! ECONAZOLE NITRATE CREAM [PRASCO LABORATORIES]
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ECONAZOLE NITRATE cream
[Prasco Laboratories]


Category DEA Schedule Marketing Status
HUMAN PRESCRIPTION DRUG LABEL Abbreviated New Drug Application
Drug Label Sections


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Prescribing Information

DESCRIPTION:

Econazole Nitrate Cream 1% contains the antifungal agent, econazole nitrate 1% in a water miscible base consisting of pegoxol 7 stearate, peglicol 5 oleate, mineral oil, benzoic acid, butylated hydroxyanisole, and purified water. The white to off-white soft cream is for topical use only.

Chemically, econazole nitrate is 1-[2-{(4-chlorophenyl) methoxy}-2-(2,4- dichlorophenyl)ethyl]-1H-imidazole mononitrate. Its structure is as follows:

Chemical Structure

CLINICAL PHARMACOLOGY:

After topical application to the skin of normal subjects, systemic absorption of econazole nitrate is extremely low. Although most of the applied drug remains on the skin surface, drug concentrations were found in the stratum corneum which, by far, exceeded the minimum inhibitory concentration for dermatophytes. Inhibitory concentrations were achieved in the epidermis and as deep as the middle region of the dermis. Less than 1% of the applied dose was recovered in the urine and feces.

Microbiology: Econazole nitrate has been shown to be active against most strains of the following microorganisms, both in vitro and in clinical infections as described in the INDICATIONS AND USAGE section.

FOR TOPICAL DERMATOLOGIC USE ONLY - NOT FOR OPHTHALMIC, ORAL, OR INTRAVAGINAL USE.

Dermatophytes                                        Yeasts

Epidermophyton floccosum                 Candida albicans

Microsporum audouini                        Malassezia furfur

Microsporum canis

Microsporum gypseum

Trichophyton mentagrophytes

Trichophyton rubrum

Trichophyton tonsurans

Econazole nitrate exhibits broad-spectrum antifungal activity against the following organisms in vitro, but the clinical significance of these data is unknown.

Dermatophytes                                         Yeasts

Trichophyton verrucosum                    Candida guillermondii

                                                             Candida parapsilosis

                                                             Candida tropicalis


INDICATIONS AND USAGE:

ECONAZOLE NITRATE CREAM 1% is indicated for topical application in the treatment of tinea pedis, tinea cruris, and tinea corporis caused by Trichophyton rubrum, Trichophyton mentagrophytes, Trichophyton tonsurans, Microsporum canis, Microsporum audouini, Microsporum gypseum, and Epidermophyton floccosum, in the treatment of cutaneous candidiasis, and in the treatment of tinea versicolor.

CONTRAINDICATIONS:

ECONAZOLE NITRATE CREAM 1% is contraindicated in individuals who have shown hypersensitivity to any of its ingredients.

WARNINGS:

ECONAZOLE NITRATE CREAM 1% is not for ophthalmic use.

PRECAUTIONS:

General: If a reaction suggesting sensitivity or chemical irritation should occur, use of the medication should be discontinued.

For external use only. Avoid introduction of ECONAZOLE NITRATE CREAM 1% into the eyes.

Carcinogenicity Studies: Long-term animal studies to determine carcinogenic potential have not been performed.

Fertility (Reproduction): Oral administration of econazole nitrate in rats has been reported to produce prolonged gestation. Intravaginal administration in humans has not shown prolonged gestation or other adverse reproductive effects attributable to econazole nitrate therapy.

Pregnancy: Pregnancy Category C. Econazole nitrate has not been shown to be teratogenic when administered orally to mice, rabbits, or rats. Fetotoxic or embryotoxic effects were observed in Segment I oral studies with rats receiving 10 to 40 times the human dermal dose. Similar effects were observed in Segment II or Segment III studies with mice, rabbits and/or rats receiving oral doses 80 or 40 times the human dermal dose. Econazole nitrate should be used in the first trimester of pregnancy only when the physician considers it essential to the welfare of the patient. The drug should be used during the second and third trimesters of pregnancy only if clearly needed.

Nursing Mothers: It is not known whether econazole nitrate is excreted in human milk. Following oral administration of econazole nitrate to lactating rats, econazole and/or metabolites were excreted in milk and were found in nursing pups. Also, in lactating rats receiving large oral doses (40 or 80 times the human dermal dose), there was a reduction in post partum viabliity of pups and survival to weaning; however, at these high doses, maternal toxicity was present and may have been a contributing factor. Caution should be exercised when econazole nitrate is administered to a nursing woman.

ADVERSE REACTIONS:

During clinical trials, approximately 3% of patients treated with econazole nitrate 1% cream reported side effects thought possibly to be due to the drug, consisting mainly of burning, itching, stinging, and erythema. One case of pruritic rash has also been reported.

OVERDOSE:

Overdosage of econzole nitrate in humans has not been reported to date. In mice, rats, guinea pigs and dogs, the oral LD50 values were found to be 462, 668, 272, and > 160 mg/kg, respectively.

DOSAGE AND ADMINISTRATION:

Sufficient ECONAZOLE NITRATE CREAM 1% should be applied to cover affected areas once daily in patients with tinea pedis, tinea cruris, tinea corporis, and tinea versicolor, and twice daily (morning and evening) in patients with cutaneous candidiasis. Early relief of symptoms is experienced by the majority of patients and clinical improvement may be seen fairly soon after treatment is begun; however, candidal 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 the treatment period, the diagnosis should be redetermined. Patients with tinea versicolor usually exhibit clinical and mycological clearing after two weeks of treatment.

HOW SUPPLIED:

ECONAZOLE NITRATE CREAM 1% is supplied in tubes of 15 grams (NDC 66993-879-15), 30 grams (NDC 66993-879-31), and 85 grams (NDC 66993-879-85).


Store at controlled room temperature 20°-25°C (68°-77°F).

128914-0509

Manufactured by:

DPT Laboratories, Ltd.

San Antonio, Texas 78215


Manufactured for:

Prasco Laboratories

Mason, OH 45040 USA

Prasco Logo


Econazole 15 g Carton

Econazole 15g Tube

Econazole 30g Carton

Econazole 30g Tube

Econazole 85 g Carton

Econazole 85g Tube
ECONAZOLE NITRATE 
econazole nitrate cream
Product Information
Product TypeHUMAN PRESCRIPTION DRUG LABELItem Code (Source)NDC:66993-879
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ECONAZOLE NITRATE (ECONAZOLE) ECONAZOLE NITRATE10 mg  in 1 g
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66993-879-1515 g in 1 TUBE
2NDC:66993-879-3130 g in 1 TUBE
3NDC:66993-879-8585 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07657409/01/200702/28/2015
Labeler - Prasco Laboratories (065969375)

Revised: 9/2013
 
Prasco Laboratories

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