Label: KETACONAZOLE- ketaconazole aerosol, foam

  • NDC Code(s): 0378-7007-01, 0378-7007-50
  • Packager: Mylan Pharmaceuticals Inc.
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application Authorized Generic

Drug Label Information

Updated September 30, 2018

If you are a consumer or patient please visit this version.

  • HIGHLIGHTS OF PRESCRIBING INFORMATION
    These highlights do not include all the information needed to use KETOCONZOLE FOAM safely and effectively. See full prescribing information for KETOCONZOLE FOAM.
     
    KETOCONZOLE foam, 2%
    For topical use

    Initial U.S. Approval: 1981

    INDICATIONS AND USAGE

    Ketoconazole foam is indicated for topical treatment of seborrheic dermatitis in immunocompetent patients 12 years of age and older (1).

    Limitations of Use

    Safety and efficacy of ketoconazole foam for treatment of fungal infections have not been established.

    DOSAGE AND ADMINISTRATION

    Ketoconazole foam should be applied to the affected area(s) twice daily for four weeks ( 2).
    Ketoconazole foam is not for ophthalmic, oral, or intravaginal use ( 2).

    DOSAGE FORMS AND STRENGTHS

    Foam: 2% ketoconazole in 50 g and 100 g containers (3).

    CONTRAINDICATIONS

    None.

    WARNINGS AND PRECAUTIONS

    Ketoconazole foam may result in contact sensitization, including photoallergenicity ( 5.1, 6.2).
    The contents of ketoconazole foam are flammable. Avoid fire, flame, or smoking during and immediately following application ( 5.2).

    ADVERSE REACTIONS

    The most common adverse reactions observed in clinical studies (incidence > 1%) were application site burning and application site reaction (6.1).

    To report SUSPECTED ADVERSE REACTIONS, contact Mylan at 1-877-446-3679 (1-877-4-INFO-RX) or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

    See 17 for PATIENT COUNSELING INFORMATION and FDA-approved patient labeling.

    Revised: 9/2018

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  • FULL PRESCRIBING INFORMATION: CONTENTS*
  • 1 INDICATIONS AND USAGE

    Ketoconazole foam, 2% is indicated for the topical treatment of seborrheic dermatitis in immunocompetent patients 12 years of age and older.

    Limitations of Use

    Safety and efficacy of ketoconazole foam for treatment of fungal infections have not been established.

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  • 2 DOSAGE AND ADMINISTRATION

    Ketoconazole foam should be applied to the affected area(s) twice daily for four weeks.

    Hold the container upright, and dispense ketoconazole foam into the cap of the can or other cool surface in an amount sufficient to cover the affected area(s). Dispensing directly onto hands is not recommended, as the foam will begin to melt immediately upon contact with warm skin. Pick up small amounts of ketoconazole foam with the fingertips, and gently massage into the affected area(s) until the foam disappears. For hair-bearing areas, part the hair, so that ketoconazole foam may be applied directly to the skin (rather than on the hair).

    Avoid contact with the eyes and other mucous membranes. Ketoconazole foam is not for ophthalmic, oral or intravaginal use.

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  • 3 DOSAGE FORMS AND STRENGTHS

    Ketoconazole foam, 2% contains 20 mg of ketoconazole, USP per gram, supplied in 50 g and 100 g containers.

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  • 4 CONTRAINDICATIONS

    None.

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  • 5 WARNINGS AND PRECAUTIONS

    5.1 Contact Sensitization

    Ketoconazole foam may result in contact sensitization, including photoallergenicity [see Adverse Reactions (6.2)].

    5.2 Flammable Contents

    The contents of ketoconazole foam include alcohol and propane/butane, which are flammable. Avoid fire, flame and/or smoking during and immediately following application. Do not puncture and/or incinerate the containers. Do not expose containers to heat and/or store at temperatures above 120°F (49°C).

    5.3 Systemic Effects

    Hepatitis has been seen with orally administered ketoconazole (1:10,000 reported incidence). Lowered testosterone and ACTH–induced corticosteroid serum levels have been seen with high doses of orally administered ketoconazole. These effects have not been seen with topical ketoconazole.

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  • 6 ADVERSE REACTIONS

    6.1 Clinical Trials Experience

    Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug, and may not reflect the rates observed in practice. The adverse reaction information from clinical trials does, however, provide a basis for identifying the adverse reactions that appear to be related to drug use and for approximating rates.

    The safety data presented in Table 1 reflect exposure to ketoconazole foam in 672 subjects, 12 years and older with seborrheic dermatitis. Subjects applied ketoconazole foam or vehicle foam twice daily for 4 weeks to affected areas on the face, scalp, and/or chest. Adverse reactions occurring in > 1% of subjects are presented in Table 1.

    Table 1: Adverse Reactions Reported by > 1% Subjects in Clinical Trials

    Adverse
    Reactions

    Ketoconazole Foam
    N = 672
    n (%)

    Vehicle Foam
    N = 497
    n (%)

    Subjects with an
    Adverse Reaction

    188 (28%)

    122 (25%)

    Application site burning

    67 (10%)

    49 (10%)

    Application site reaction

    41 (6%)

    24 (5%)

    Application site reactions that were reported in < 1% of subjects were dryness, erythema, irritation, paresthesia, pruritus, rash and warmth.

    6.2 Dermal Safety Studies

    In a photoallergenicity study, 9 of 53 subjects (17%) had reactions during the challenge period at both the irradiated and non-irradiated sites treated with ketoconazole foam. Ketoconazole foam may cause contact sensitization.

    6.3 Postmarketing Experience

    The following adverse events have been identified during postmarketing use of ketoconazole foam:

    Gastrointestinal disorders: Cheilitis

    General disorders and administration site conditions: Application site pain and application site burn

    Skin and subcutaneous tissue disorders: Skin burning sensation and erythema

    Because these events are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

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  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary

    There are no available data on ketoconazole foam use in pregnant women to identify a drug-associated risk of major birth defects, miscarriage or adverse maternal or fetal outcomes. No reproductive studies in animals have been performed with ketoconazole foam. In animal reproduction studies with pregnant mice, rats and rabbits both embryotoxic and developmental effects (structural abnormalities) were observed following oral dosing of ketoconazole during organogenesis. Assuming equivalent systemic absorption of topical and oral ketoconazole doses and an ketoconazole foam maximum recommended human dose (MRHD) of 8 grams (equivalent to 160 mg ketoconazole), embryotoxic effects were observed at 0.8 to 2.4 times the MRHD and developmental effects were observed at 4.8 times the MRHD [see Data].

    The background risk of major birth defects and miscarriage for the indicated population is unknown. All pregnancies have a background risk of birth defect, loss, or other adverse outcomes. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2 to 4% and 15 to 20%, respectively.

    Data

    Animal Data

    The animal multiples of human exposure calculations are based on body surface area (BSA) comparisons of oral doses administered to animals and an ketoconazole foam maximum recommended human dose (MRHD) of 8 grams (equivalent to 2.67 mg ketoconazole/kg/day for a 60 kg individual or 98.8 mg ketoconazole/m2/day).

    Embryofetal development studies have been conducted in mice, rats and rabbits with orally administered ketoconazole. When orally administered to mice on gestational days 6 through 18 (covering the period of organogenesis), ketoconazole was embryotoxic (25 mg/kg and higher; 0.8 times the MRHD based on BSA comparisons) with a high incidence of resorptions, increased number of stillbirths and delayed parturition. Delays in maturation were also observed. There was no evidence of maternal toxicity or malformations at up to 50 mg/kg (1.5 times the MRHD based on BSA comparisons). No treatment related developmental effects were observed at 10 mg/kg (0.3 times the MRHD based on BSA comparisons).

    In the presence of maternal toxicity in rats, orally administered ketoconazole was both embryotoxic (40 mg/kg and higher; 2.4 times the MRHD based on BSA comparisons), including increased resorbed fetuses and stillbirths, and teratogenic (80 mg/kg and higher; 4.8 times the MRHD based on BSA comparisons), including syndactylia, oligodactylia, waved ribs and cleft palate. Additionally, 100 mg/kg (6 times the MRHD based on BSA comparisons) ketoconazole orally administered on a single day during gestation (gestational days 9 through 12) was embryotoxic (increased resorptions). This same oral dose given on gestation day 12, 13, 14 or 15 induced external malformations including cleft palate, micromelia and digital anomalies (brachydactyly, ectrodactyly, syndactyly).

    In pregnant rabbits orally administered ketoconazole, evidence of embryotoxicity (increased resorptions) was observed at 10 mg/kg (1.2 times the MRHD based on BSA comparisons) and higher and an increased incidence of skeletal abnormalities was observed at 40 mg/kg (4.8 times the MRHD based on BSA comparisons).

    8.2 Lactation

    Risk Summary

    There is no information available on the presence of ketoconazole in human milk, or the effects on the breastfed child, or the effects on milk production after topical application of ketoconazole foam to women who are breastfeeding. In animal studies ketoconazole was found in milk following oral administration. The developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for ketoconazole foam and any potential adverse effects on the breastfed infant from ketoconazole foam or from the underlying maternal condition.

    8.3 Females and Males of Reproductive Potential

    Infertility

    In animal fertility studies in rats and dogs, administration of oral doses of ketoconazole between 3-day and 3-month periods resulted in infertility that was reversible [see Nonclinical Toxicology (13.1)].

    8.4 Pediatric Use

    The safety and effectiveness of ketoconazole foam in pediatric patients less than 12 years of age have not been established.

    Of the 672 subjects treated with ketoconazole foam in the clinical trials, 44 (7%) were from 12 to 17 years of age. [See Clinical Studies (14)].

    8.5 Geriatric Use

    Of the 672 subjects treated with ketoconazole foam in the clinical trials, 107 (16%) were 65 years and over. Clinical trials of ketoconazole foam did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently than younger subjects.

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  • 11 DESCRIPTION

    Ketoconazole foam contains 2% ketoconazole USP, an antifungal agent, in a thermolabile hydroethanolic foam for topical application.

    The chemical name for ketoconazole is piperazine, 1-acetyl-4-[4-[[2-(2,4-dichlorophenyl) -2-(1H-imidazol-l-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]-, cis- with the molecular formula C26H28Cl2N4O4 and a molecular weight of 531.43. The following is the chemical structure:

    Ketoconazole Structural Formula

    Ketoconazole foam contains 20 mg of ketoconazole per gram in a thermolabile hydroethanolic foam vehicle consisting of cetyl alcohol, citric acid, ethanol (denatured with tert-butyl alcohol and brucine sulfate) 58%, polysorbate 60, potassium citrate, propylene glycol, purified water, and stearyl alcohol pressurized with a hydrocarbon (propane/butane) propellant.

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  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    The mechanism of action of ketoconazole in the treatment of seborrheic dermatitis is not known.

    12.2 Pharmacodynamics

    The pharmacodynamics of ketoconazole foam has not been established.

    12.3 Pharmacokinetics

    In a bioavailability study, 12 subjects with moderate to severe seborrheic dermatitis applied 3 g of ketoconazole foam twice daily for 4 weeks. Circulating plasma levels of ketoconazole were < 6 ng/mL for a majority of subjects (75%), with a maximum level of 11 ng/mL observed in one subject.

    12.4 Microbiology

    Ketoconazole is an antifungal agent which inhibits the in vitro synthesis of ergosterol, a key sterol in the cell membrane of Malassezia furfur. The clinical significance of antifungal activity in the treatment of seborrheic dermatitis is not known.

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  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    Long-term animal studies have not been performed to evaluate the carcinogenic or photo-carcinogenic potential of ketoconazole foam.

    In oral carcinogenicity studies in mice (18-months) and rats (24-months) at dose levels of 5, 20 and 80 mg/kg/day ketoconazole was not carcinogenic. The high dose in these studies was approximately 2.4 to 4.8 times the MRHD based on BSA comparisons. In a bacterial reverse mutation assay, ketoconazole did not express any mutagenic potential. In three in vivo assays (sister chromatid exchange in humans, dominant lethal and micronucleus tests in mice), ketoconazole did not exhibit any genotoxic potential.

    In animal fertility studies, oral ketoconazole impaired both male and female fertility in rats in a dose and duration dependent manner. In females, oral doses up to 40 mg/kg (2.4 times the MRHD based on BSA comparisons) had no effect on fertility, while doses of 75 mg/kg (4.5 times the MRHD based on BSA comparisons) and higher decreased the pregnancy rate and number of implantation sites. In male rats, oral dosing at 200 mg/kg/day (12 times the MRHD based on BSA comparisons) for three days decreased fertility and 400 mg/kg/day (24 times the MRHD based on BSA comparisons) for three days resulted in a complete loss of fertility. When administered for longer durations (up to 3 months), decreased fertility in male rats was observed at doses as low as 24 mg/kg/day (1.4 times the MRHD based on BSA comparisons). In male beagle dogs, an oral dose of 25 mg/kg/day ketoconazole for up to 4 weeks (5.2 times the MRHD based on BSA comparisons) resulted in decreased sperm motility, decreased sperm count, increased abnormal sperm and atrophy of the testes. These effects were reversed subsequent to withdrawal of treatment.

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  • 14 CLINICAL STUDIES

    The safety and efficacy of ketoconazole foam were evaluated in a randomized, double-blind, vehicle-controlled trial in subjects 12 years and older with mild to severe seborrheic dermatitis. In the trial, 427 subjects received ketoconazole foam and 420 subjects received vehicle foam. Subjects applied ketoconazole foam or vehicle foam twice daily for 4 weeks to affected areas on the face, scalp, and/or chest. The overall disease severity in terms of erythema, scaling, and induration was assessed at Baseline and week 4 on a 5-point Investigator’s Static Global Assessment (ISGA) scale.

    Treatment success was defined as achieving a Week 4 (end of treatment) ISGA score of 0 (clear) or 1 (majority of lesions have individual scores for scaling, erythema, and induration that averages 1 [minimal or faint]) and at least two grades of improvement from baseline. The results are presented in Table 2. The database was not large enough to assess whether there were differences in effects in age, gender, or race subgroups.

    Table 2: Efficacy Results

    Number of Subjects

    Ketoconazole Foam
    N = 427
    n (%)

    Vehicle Foam
    N = 420
    n (%)

    Subjects Achieving
    Treatment Success


    239 (56%)


    176 (42%)

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  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    Ketoconazole Foam, 2% contains 20 mg of ketoconazole, USP per gram. The thermolabile hydroethanolic foam is available as follows:

    NDC 0378-7007-50
    50 g aluminum can

    NDC 0378-7007-01
    100 g aluminum can

    Store at 20° to 25°C (68° to 77°F). [See USP Controlled Room Temperature.]

    Do not store under refrigerated conditions.

    Contents are flammable. Do not expose containers to heat and/or store at temperatures above 49°C (120°F). Do not store in direct sunlight.

    Contents under pressure. Do not puncture and/or incinerate container.

    Keep out of reach of children.

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  • 17 PATIENT COUNSELING INFORMATION

    See FDA-approved patient labeling (Patient Package Insert).

    Instruct patients on a proper use of ketoconazole foam

    Avoid fire, flame and/or smoking during and immediately following application.
    Do not apply ketoconazole foam directly to hands. Dispense onto a cool surface, and apply to the affected areas using the fingertips.
    Wash their hands after application
    Ketoconazole foam may cause skin irritation (application site burning and/or reactions)
    Instruct a patient to contact a health care provider if the area of application shows signs of increased irritation and report any signs of adverse reactions.
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  • PATIENT INFORMATION

    Ketoconazole Foam
    (kee″ toe kon′ a zole)

    Important Information: Ketoconazole foam is for use on the skin only. Do not use ketoconazole foam in your eyes, mouth or vagina.

    What is ketoconazole foam?

    Ketoconazole foam is a prescription medicine used on the skin (topical) to treat seborrheic dermatitis in people 12 years of age and older with a normal immune system.

     

    It is not known if ketoconazole foam is safe and effective when used to treat fungal infections.

     

    It is not known if ketoconazole foam is safe and effective in children less than 12 years of age.

    Before using ketoconazole foam, tell your healthcare provider about all of your medical conditions, including if you:

    are pregnant or plan to become pregnant. It is not known if ketoconazole foam will harm your unborn baby.
    are breastfeeding or plan to breastfeed. It is not known if ketoconazole passes into your breast milk. Talk to your healthcare provider about the best way to feed your baby during treatment with ketoconazole foam.

    Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.

    How should I use ketoconazole foam?

    Use ketoconazole foam exactly as your healthcare provider tells you to use it. See the detailed “Instructions for Use” at the end of this leaflet for directions about how to apply ketoconazole foam the right way.
    Apply ketoconazole foam to the affected skin area(s) 2 times each day for 4 weeks. You should apply enough ketoconazole foam to cover the entire affected area(s).
    Talk to your healthcare provider if your skin does not improve after 4 weeks of treatment with ketoconazole foam.
    Dispense ketoconazole foam directly into the cap. Do not dispense ketoconazole foam directly onto your hands, because the foam will begin to melt on contact with warm skin.
    Wash your hands after applying ketoconazole foam.

    What should I avoid while using ketoconazole foam?

    Ketoconazole foam is flammable. Avoid fire, flames, or smoking during and right after you apply ketoconazole foam to your skin.
    Avoid getting ketoconazole foam in or near your eyes, mouth, lips or vagina. If you get ketoconazole foam on your lips or in your eyes, mouth or vagina, rinse well with water.

    What are the possible side effects of ketoconazole foam?

     

    Ketoconazole foam may cause serious side effects, including:

    Skin irritation at the application area(s), including skin reactions caused by exposure to light. Tell your healthcare provider if you develop skin irritation during treatment with ketoconazole foam.

    The most common side effects of ketoconazole foam include, burning, dryness, redness, irritation, numbness, itching, rash and warmth at the application site.

     

    These are not all of the possible side effects of ketoconazole foam.

     

    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 ketoconazole foam?

    Store ketoconazole foam at room temperature between 68°F to 77°F (20°C to 25°C).
    Do not store the ketoconazole foam can in the refrigerator or freezer.
    Keep ketoconazole foam away from heat. Never throw the ketoconazole foam can into a fire, even if the can is empty.
    Do not store ketoconazole foam at temperatures above 120°F (49°C).
    Do not break through (puncture) the ketoconazole foam can.

    Keep ketoconazole foam and all medicines out of the reach of children.

    General information about the safe and effective use of ketoconazole foam.

    Medicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet. Do not use ketoconazole foam for a condition for which it was not prescribed. Do not give ketoconazole foam 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 ketoconazole foam that is written for health professionals.

    What are the ingredients in ketoconazole foam?

    Active ingredient: ketoconazole

    Inactive ingredients: cetyl alcohol, citric acid, ethanol (denatured with tert-butyl alcohol and brucine sulfate) 58%, polysorbate 60, potassium citrate, propylene glycol, purified water, and stearyl alcohol pressurized with a hydrocarbon (propane/butane) propellant

     

    Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A.

     

    For more information, call Mylan at 1-877-446-3679 (1-877-4-INFO-RX).

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

     

     

    INSTRUCTIONS FOR USE

    Ketoconazole Foam
    (kee″ toe kon′ a zole)

    Important Information: Ketoconazole foam is for use on the skin only. Do not use ketoconazole foam in your eyes, mouth or vagina.

     
    Step 1: Remove the clear cap from the ketoconazole foam can.
    Instructions for Use Figure 01
     
    Step 2: Hold the can upright and firmly press the nozzle to dispense ketoconazole foam into the clear cap.
    Dispense enough ketoconazole foam to cover the entire affected area(s).
    Instructions for Use Figure 02
    If the can seems warm or the foam seems runny, run the can under cold water.
    Instructions for Use Figure 03
     
    Step 3: Pick up small amounts of ketoconazole foam with your fingertips and gently rub the foam into the affected area(s) until the foam disappears.
    Instructions for Use Figure 04

     

    Instructions for Use Figure 05
    If you are treating areas such as your scalp, part the hair so that ketoconazole foam may be applied directly to the skin.
    Instructions for Use Figure 06
     
    Step 4: Wash your hands after applying ketoconazole foam.
    Throw away any of the unused medicine that is left in the cap.
    Instructions for Use Figure 07

    How should I store ketoconazole foam?

    Store ketoconazole foam at room temperature between 68°F to 77°F (20°C to 25°C).
    Do not store the ketoconazole foam can in the refrigerator or freezer.
    Keep ketoconazole foam away from heat. Never throw the can into a fire, even if the can is empty.
    Do not store ketoconazole foam at temperatures above 120°F (49°C).
    Do not break through (puncture) the ketoconazole foam can.

    Keep ketoconazole foam and all medicines out of the reach of children.

    This Instructions for Use has been approved by the U.S. Food and Drug Administration.

    Manufactured for:
    Mylan Pharmaceuticals Inc.
    Morgantown, WV 26505 U.S.A.

    Manufactured by:
    DPT Laboratories, Ltd.
    San Antonio, TX 78215 U.S.A.

    141031-0918

    Revised: 9/2018
    DPT:KTCZFOG:R1

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  • PRINCIPAL DISPLAY PANEL – 2%

    NDC 0378-7007-50

    Ketoconazole
    Foam
    2%

    FOR TOPICAL USE ONLY

    Rx only 50 g

    NOT FOR OPHTHALMIC, ORAL,
    OR INTRAVAGINAL USE.

    Ketoconazole 2% Carton Image

    Hold the can at an
    upright angle and
    then press firmly
    to dispense.

    Description: Ketoconazole Foam, 2%
    contains 20 mg of ketoconazole, USP
    per gram in a thermolabile hydroethanolic
    foam vehicle consisting of cetyl alcohol,
    citric acid, ethanol (denatured with
    tert-butyl alcohol and brucine sulfate)
    58%, polysorbate 60, potassium citrate,
    propylene glycol, purified water,
    stearyl alcohol pressurized with a
    hydrocarbon (propane/butane)
    propellant.

    Usual Dosage: Use only as prescribed
    by your physician. See accompanying
    prescribing information.

    Warning: FLAMMABLE. AVOID FIRE,
    FLAME, OR SMOKING DURING AND
    IMMEDIATELY FOLLOWING
    APPLICATION.

    Contents under pressure. Do not puncture
    and/or incinerate container. Do not
    expose containers to heat and/or store
    at temperatures above 120ºF (49ºC).

    Do not store in direct sunlight.

    Avoid contact with eyes. Keep this
    and all medication out of the reach
    of children.

    Do not store in the refrigerator.
    Store at 20º to 25ºC (68º to 77ºF).
    [See USP Controlled Room Temperature.]

    CFC FREE

    Manufactured for:
    Mylan Pharmaceuticals Inc.
    Morgantown, WV 26505 U.S.A.

    Manufactured by:
    DPT Laboratories, Ltd.
    San Antonio, TX 78215 U.S.A.

    For more information, call
    Mylan at 1-877-446-3679
    (1-877-4-INFO-RX)

    117545-0918
    DPT:7007:50:1C:R1

    Mylan.com

    Ketoconazole Foam 2% Carton Label
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  • INGREDIENTS AND APPEARANCE
    KETACONAZOLE 
    ketaconazole aerosol, foam
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0378-7007
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    KETOCONAZOLE (UNII: R9400W927I) (KETOCONAZOLE - UNII:R9400W927I) KETOCONAZOLE 20 mg  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ALCOHOL (UNII: 3K9958V90M)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    POTASSIUM CITRATE (UNII: EE90ONI6FF)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0378-7007-50 1 in 1 CARTON 12/20/2018
    1 50 g in 1 CAN; Type 0: Not a Combination Product
    2 NDC:0378-7007-01 1 in 1 CARTON 12/20/2018
    2 100 g in 1 CAN; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA authorized generic NDA021738 12/20/2018
    Labeler - Mylan Pharmaceuticals Inc. (059295980)
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