LOTRISONE- clotrimazole and betamethasone dipropionate cream

Lotrisone by

Drug Labeling and Warnings

Lotrisone by is a Prescription medication manufactured, distributed, or labeled by Merck Sharp & Dohme Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • 1 INDICATIONS AND USAGE

    LOTRISONE® cream is a combination of an azole antifungal and corticosteroid and is indicated for the topical treatment of symptomatic inflammatory tinea pedis, tinea cruris, and tinea corporis due to Epidermophyton floccosum, Trichophyton mentagrophytes, and Trichophyton rubrum in patients 17 years and older.

  • 2 DOSAGE AND ADMINISTRATION

    Treatment of tinea corporis or tinea cruris:

    • Apply a thin film of LOTRISONE cream into the affected skin areas twice a day for one week.
    • Do not use more than 45 grams per week. Do not use with occlusive dressings.
    • If a patient shows no clinical improvement after 1 week of treatment with LOTRISONE cream, the diagnosis should be reviewed.
    • Do not use longer than 2 weeks.

    Treatment of tinea pedis:

    • Gently massage a sufficient amount of LOTRISONE cream into the affected skin areas twice a day for two weeks.
    • Do not use more than 45 grams per week. Do not use with occlusive dressings.
    • If a patient shows no clinical improvement after 2 weeks of treatment with LOTRISONE cream, the diagnosis should be reviewed.
    • Do not use longer than 4 weeks.

    LOTRISONE cream is for topical use only. It is not for oral, ophthalmic, or intravaginal use.

    Avoid contact with eyes. Wash hands after each application.

  • 3 DOSAGE FORMS AND STRENGTHS

    Cream, 1%/0.05%. Each gram of LOTRISONE cream contains 10 mg of clotrimazole and 0.643 mg of betamethasone dipropionate (equivalent to 0.5 mg of betamethasone) in a white to off-white cream base.

  • 4 CONTRAINDICATIONS

    None.

  • 5 WARNINGS AND PRECAUTIONS

    5.1 Effects on Endocrine System

    LOTRISONE cream can cause reversible hypothalamic-pituitary-adrenal (HPA) axis suppression with the potential for glucocorticosteroid insufficiency. This may occur during treatment or after withdrawal of treatment. Cushing's syndrome and hyperglycemia may also occur due to the systemic effect of corticosteroids while on treatment. Factors that predispose a patient to HPA axis suppression include the use of high-potency steroids, large treatment surface areas, prolonged use, use of occlusive dressing, altered skin barrier, liver failure, and young age.

    Because of the potential for systemic corticosteroid effects, patients may need to be periodically evaluated for HPA axis suppression. This may be done by using the adrenocorticotropic hormone (ACTH) stimulation test.

    In a small trial, LOTRISONE cream was applied using large dosages, 7 g daily for 14 days (BID) to the crural area of normal adult subjects. Three of the 8 normal subjects on whom LOTRISONE cream was applied exhibited low morning plasma cortisol levels during treatment. One of these subjects had an abnormal cosyntropin test. The effect on morning plasma cortisol was transient and subjects recovered 1 week after discontinuing dosing. In addition, 2 separate trials in pediatric subjects demonstrated adrenal suppression as determined by cosyntropin testing [see Use in Specific Populations (8.4)].

    If HPA axis suppression is documented, gradually withdraw the drug, reduce the frequency of application, or substitute with a less potent corticosteroid.

    Pediatric patients may be more susceptible to systemic toxicity due to their larger skin-surface-to-body mass ratios [see Use in Specific Populations (8.4)].

    5.2 Diaper Dermatitis

    The use of LOTRISONE cream in the treatment of diaper dermatitis is not recommended.

    5.3 Ophthalmic Adverse Reactions

    Use of topical corticosteroids may increase the risk of posterior subcapsular cataracts and glaucoma. Cataracts and glaucoma have been reported in postmarketing experience with the use of topical corticosteroid products, including topical betamethasone products [see Adverse Reactions (6.2)].

    Avoid contact of LOTRISONE cream with eyes. Advise patients to report any visual symptoms and consider referral to an ophthalmologist for evaluation.

  • 6 ADVERSE REACTIONS

    6.1 Clinical Trial 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.

    In clinical trials common adverse reaction reported for LOTRISONE cream was paresthesia in 1.9% of patients. Adverse reactions reported at a frequency < 1% included rash, edema, and secondary infection.

    6.2 Postmarketing Experience

    Because adverse reactions 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.

    The following local adverse reactions have been reported with topical corticosteroids: itching, irritation, dryness, folliculitis, hypertrichosis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, maceration of the skin, skin atrophy, striae, miliaria, capillary fragility (ecchymoses), telangiectasia, and sensitization (local reactions upon repeated application of product).

    Ophthalmic adverse reactions of blurred vision, cataracts, glaucoma, increased intraocular pressure, and central serous chorioretinopathy have been reported with the use of topical corticosteroids, including topical betamethasone products.

    Adverse reactions reported with the use of clotrimazole are: erythema, stinging, blistering, peeling, edema, pruritus, urticaria, and general irritation of the skin.

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary

    There are no available data on topical betamethasone dipropionate or clotrimazole use in pregnant women to identify a LOTRISONE cream associated risk of major birth defects, miscarriage, or adverse maternal or fetal outcomes.

    Observational studies suggest an increased risk of low birthweight infants with the use of potent or very potent topical corticosteroid during pregnancy. Advise pregnant women that LOTRISONE cream may increase the risk of having a low birthweight infant and to use LOTRISONE cream on the smallest area of skin and for the shortest duration possible.

    There have been no reproduction studies performed in animals or humans with the combination of clotrimazole and betamethasone dipropionate. In an animal reproduction study, betamethasone dipropionate caused malformations (i.e., umbilical hernias, cephalocele, and cleft palate) in pregnant rabbits when given by the intramuscular route during organogenesis [see Data]. The available data do not allow the calculation of relevant comparisons between the systemic exposure of clotrimazole and/or betamethasone dipropionate observed in the animal studies to the systemic exposure that would be expected in humans after topical use of LOTRISONE cream.

    The estimated 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 risk of major birth defects and miscarriage in clinically recognized pregnancies is 2 to 4% and 15 to 20%, respectively.

    Data

    Animal Data

    Clotrimazole

    Studies in pregnant rats treated during organogenesis with intravaginal doses up to 100 mg/kg/day revealed no evidence of fetotoxicity due to clotrimazole exposure.

    No increase in fetal malformations was noted in pregnant rats receiving oral (gastric tube) clotrimazole doses up to 100 mg/kg/day during gestation Days 6 to 15. However, clotrimazole dosed at 100 mg/kg/day was embryotoxic (increased resorptions), fetotoxic (reduced fetal weights), and maternally toxic (reduced body weight gain) to rats. Clotrimazole dosed at 200 mg/kg/day was maternally lethal, and therefore, fetuses were not evaluated in this group. Also in this study, doses up to 50 mg/kg/day had no adverse effects on dams or fetuses. However, in the combined fertility, embryofetal development, and postnatal development study conducted in rats, 50 mg/kg/day clotrimazole was associated with reduced maternal weight gain and reduced numbers of offspring reared to 4 weeks [see Nonclinical Toxicology (13.1)].

    Oral clotrimazole doses of 25, 50, 100, and 200 mg/kg/day did not cause malformations in pregnant mice. No evidence of maternal toxicity or embryotoxicity was seen in pregnant rabbits dosed orally during organogenesis with 60, 120, or 180 mg/kg/day.

    Betamethasone Dipropionate

    Betamethasone dipropionate caused malformations when given to pregnant rabbits during organogenesis by the intramuscular route at doses of 0.05 mg/kg/day. The abnormalities observed included umbilical hernias, cephalocele, and cleft palates.

    8.2 Lactation

    Risk Summary

    There are no data regarding the excretion of betamethasone dipropionate or clotrimazole into breast milk, the effects on the breastfed infant, or the effects on milk production after topical application to women who are breastfeeding.

    It is possible that topical administration of betamethasone dipropionate could result in sufficient systemic absorption to produce detectable quantities in human milk. The developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for LOTRISONE cream and any potential adverse effects on the breastfed infant from LOTRISONE cream or from the underlying maternal condition.

    Clinical Considerations

    To minimize potential exposure to the breastfed infant via breast milk, use LOTRISONE cream on the smallest area of skin and for the shortest duration possible while breastfeeding. Advise breastfeeding women not to apply LOTRISONE cream directly to the nipple and areola to avoid direct infant exposure [see Use in Specific Populations (8.4)].

    8.4 Pediatric Use

    The use of LOTRISONE cream in patients under 17 years of age is not recommended.

    Adverse events consistent with corticosteroid use have been observed in pediatric patients treated with LOTRISONE cream. In open-label trials, 17 of 43 (39.5%) evaluable pediatric subjects (aged 12-16 years old) using LOTRISONE cream for treatment of tinea pedis demonstrated adrenal suppression as determined by cosyntropin testing. In another open-label trial, 8 of 17 (47.1%) evaluable pediatric subjects (aged 12-16 years old) using LOTRISONE cream for treatment of tinea cruris demonstrated adrenal suppression as determined by cosyntropin testing.

    Because of a higher ratio of skin surface area to body mass, pediatric patients are at a greater risk than adults of HPA axis suppression when they are treated with topical corticosteroids. They are, therefore also at greater risk of adrenal insufficiency during and/or after withdrawal of treatment. Pediatric patients may be more susceptible than adults to skin atrophy, including striae, when they are treated with topical corticosteroids.

    HPA axis suppression, Cushing's syndrome, linear growth retardation, delayed weight gain, and intracranial hypertension have been reported in pediatric patients receiving topical corticosteroids [see Warnings and Precautions (5.1)].

    Avoid use of LOTRISONE cream in the treatment of diaper dermatitis.

    8.5 Geriatric Use

    Clinical studies of LOTRISONE cream did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. However, greater sensitivity of some older individuals cannot be ruled out. The use of LOTRISONE cream under occlusion, such as in diaper dermatitis, is not recommended.

    Postmarket adverse event reporting for LOTRISONE cream in patients aged 65 and above includes reports of skin atrophy and rare reports of skin ulceration. Caution should be exercised with the use of these corticosteroid-containing topical products on thinning skin.

  • 11 DESCRIPTION

    LOTRISONE (clotrimazole and betamethasone dipropionate) cream, 1%/0.05%, contains combinations of clotrimazole, an azole antifungal, and betamethasone dipropionate, a corticosteroid, for topical use.

    Chemically, clotrimazole is 1–(o-chloro-α,α-diphenylbenzyl) imidazole, with the empirical formula C22H17CLN2, a molecular weight of 344.84, and the following structural formula:

    Chemical Structure

    Clotrimazole is an odorless, white crystalline powder, insoluble in water and soluble in ethanol.

    Betamethasone dipropionate has 9-fluoro-11β,17,21-trihydroxy-16β-methylpregna-1,4-diene-3,20-dione 17,21-dipropionate, with the empirical formula C28H37FO7, a molecular weight of 504.59, and the following structural formula:

    Chemical Structure

    Betamethasone dipropionate is a white to creamy-white, odorless crystalline powder, insoluble in water.

    Each gram of LOTRISONE cream contains 10 mg clotrimazole and 0.643 mg betamethasone dipropionate (equivalent to 0.5 mg betamethasone), in a white to off-white, hydrophilic cream consisting of benzyl alcohol as a preservative, ceteareth-30, cetyl alcohol plus stearyl alcohol, mineral oil, phosphoric acid, propylene glycol, purified water, sodium phosphate monobasic monohydrate, and white petrolatum.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    Clotrimazole is an azole antifungal [see Clinical Pharmacology (12.4)].

    Betamethasone dipropionate is a corticosteroid. Corticosteroids play a role in cellular signaling, immune function, inflammation, and protein regulation; however, the precise mechanism of action for the treatment of tinea pedis, tinea cruris and tinea corporis is unknown.

    12.2 Pharmacodynamics

    Vasoconstrictor Assay:

    Studies performed with LOTRISONE cream indicate that these topical combination antifungal/corticosteroids may have vasoconstrictor potencies in a range that is comparable to high-potency topical corticosteroids. However, similar blanching scores do not necessarily imply therapeutic equivalence.

    12.3 Pharmacokinetics

    Skin penetration and systemic absorption of clotrimazole and betamethasone dipropionate following topical application of LOTRISONE cream has not been studied.

    The extent of percutaneous absorption of topical corticosteroids is determined by many factors, including the vehicle, the integrity of the epidermal barrier, and the use of occlusive dressings. Topical corticosteroids can be absorbed from normal intact skin. Inflammation and/or other disease processes in the skin may increase percutaneous absorption of topical corticosteroids. Occlusive dressings substantially increase the percutaneous absorption of topical corticosteroids [see Dosage and Administration (2)].

    Once absorbed through the skin, the pharmacokinetics of topical corticosteroids are similar to systemically administered corticosteroids. Corticosteroids are bound to plasma proteins in varying degrees. Corticosteroids are metabolized primarily in the liver and are then excreted by the kidneys. Some of the topical corticosteroids and their metabolites are also excreted into the bile.

    12.4 Microbiology

    Mechanism of Action:

    Clotrimazole, an azole antifungal agent, inhibits 14-α-demethylation of lanosterol in fungi by binding to one of the cytochrome P-450 enzymes. This leads to the accumulation of 14-α-methylsterols and reduced concentrations of ergosterol, a sterol essential for a normal fungal cytoplasmic membrane. The methylsterols may affect the electron transport system, thereby inhibiting growth of fungi.

    Activity In Vitro and In Vivo:

    Clotrimazole has been shown to be active against most strains of the following dermatophytes, both in vitro and in clinical infections, Epidermophyton floccosum, Trichophyton mentagrophytes, and Trichophyton rubrum [see Indications and Usage (1)].

    Drug Resistance:

    Strains of dermatophytes having a natural resistance to clotrimazole have not been reported. Resistance to azoles, including clotrimazole, has been reported in some Candida species.

    No single-step or multiple-step resistance to clotrimazole has developed during successive passages of Trichophyton mentagrophytes.

  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    Long-term animal studies have not been performed to evaluate the carcinogenic potential of the combination of clotrimazole and betamethasone dipropionate or either component individually.

    Betamethasone was negative in the bacterial mutagenicity assay (Salmonella typhimurium and Escherichia coli) and in the mammalian cell mutagenicity assay (CHO/HGPRT). It was positive in the in vitro human lymphocyte chromosome aberration assay, and equivocal in the in vivo mouse bone marrow micronucleus assay.

    In a combined study of the effects of clotrimazole on fertility, embryofetal development, and postnatal development, male and female rats were dosed orally (diet admixture) with dose levels of 5, 10, 25, or 50 mg/kg/day from 10 weeks prior to mating until 4 weeks postpartum. No adverse effects on the duration of estrous cycle, fertility, or duration of pregnancy were noted.

    Reproductive studies with betamethasone dipropionate conducted in rabbits at doses of 1.0 mg/kg/day by the intramuscular route and in mice up to 33 mg/kg/day by the intramuscular route indicated no impairment of fertility except for dose-related increases in fetal resorption rates in both species.

  • 14 CLINICAL STUDIES

    In clinical trials of tinea corporis, tinea cruris, and tinea pedis, subjects treated with LOTRISONE cream showed a better clinical response at the first return visit than subjects treated with clotrimazole cream. In tinea corporis and tinea cruris, the subject returned 3 to 5 days after starting treatment, and in tinea pedis, after 1 week. Mycological cure rates observed in subjects treated with LOTRISONE cream were as good as, or better than, in those subjects treated with clotrimazole cream. In these same clinical studies, patients treated with LOTRISONE cream showed better clinical responses and mycological cure rates when compared with subjects treated with betamethasone dipropionate cream.

  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    LOTRISONE cream is white to off-white and supplied in 15-gram (NDC: 0085-0924-01) and 45-gram tubes (NDC: 0085-0924-02), boxes of one. Store at 20-25°C (68-77°F); excursions permitted to 15-30°C (59-86°F) [see USP Controlled Room Temperature].

    Rx only

  • 17 PATIENT COUNSELING INFORMATION

    Advise the patient to read the FDA-approved patient labeling (Patient Information).

    Inform the patient of the following:

    Pregnancy

    Advise pregnant women that LOTRISONE cream may increase the risk of having a low birthweight infant and to use LOTRISONE cream on the smallest area of skin and for the shortest duration possible [see Use in Specific Populations (8.1)].

    Lactation

    Advise a woman to use LOTRISONE cream on the smallest area of skin and for the shortest duration possible while breastfeeding. Advise breastfeeding women not to apply LOTRISONE cream directly to the nipple and areola to avoid direct infant exposure [see Use in Specific Populations (8.2)].

    Important Administration Instructions

    Inform patients of the following:

    • Use LOTRISONE cream as directed by the physician. It is for external use only.
    • Avoid contact with the eyes, the mouth, or intravaginally.
    • Advise patients to report any visual symptoms to their healthcare providers.
    • Do not use LOTRISONE cream on the face or underarms.
    • Do not use more than 45 grams of LOTRISONE cream per week.
    • When using LOTRISONE cream in the groin area, patients should use the medication for 2 weeks only, and apply the cream sparingly. Patients should wear loose-fitting clothing. Notify the physician if the condition persists after 2 weeks.
    • Do not use LOTRISONE cream for any disorder other than that for which it was prescribed.
    • Do not bandage, cover or wrap the treatment area unless directed by the physician. Avoid use of LOTRISONE cream in the diaper area, as diapers or plastic pants may constitute occlusive dressing.
    • Report any signs of local adverse reactions to the physician. Advise patients that local reactions and skin atrophy are more likely to occur with occlusive use or prolonged use.
    • This medication is to be used for the full prescribed treatment time, even though the symptoms may have improved. Notify the physician if there is no improvement after 1 week of treatment for tinea cruris or tinea corporis, or after 2 weeks for tinea pedis.
  • SPL UNCLASSIFIED SECTION

    Distributed by: Merck Sharp & Dohme Corp., a subsidiary of
    MERCK & CO., INC., Whitehouse Station, NJ 08889, USA

    For patent information: www.merck.com/product/patent/home.html

    Copyright © 1983-2019 Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.
    All rights reserved.

    uspi-mk5335A-cr-1906r005

  • PATIENT PACKAGE INSERT

    Patient Information
    LOTRISONE® (LOW-tre-zone)
    (clotrimazole and betamethasone dipropionate) cream, 1%/0.05%
    This Patient Information has been approved by the U.S. Food and Drug Administration.Revised: June 2019  
    Important information: LOTRISONE cream is for use on skin only. Do not use LOTRISONE cream in your eyes, mouth, or vagina.
    What is LOTRISONE cream?
    • LOTRISONE cream is a prescription medication used on the skin (topical) to treat fungal infections of the feet, groin, and body in people 17 years of age and older. LOTRISONE cream is used for fungal infections that are inflamed and have symptoms of redness or itching.
    • LOTRISONE cream should not be used in children under 17 years of age.
    Before using LOTRISONE cream, tell your healthcare provider about all your medical conditions, including if you:
    • are pregnant or plan to become pregnant. It is not known if LOTRISONE cream will harm your unborn baby. If you use LOTRISONE cream during pregnancy, use LOTRISONE cream on the smallest area of the skin and for the shortest time needed.
    • are breastfeeding or plan to breastfeed. It is not known if LOTRISONE cream passes into your breast milk.
      Breastfeeding women should use LOTRISONE cream on the smallest area of skin and for the shortest time needed while breastfeeding. Do not apply LOTRISONE cream directly to the nipple and areola to avoid contact with your baby.
    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 LOTRISONE cream?
    • Use LOTRISONE cream exactly as your healthcare provider tells you to use it.
    • Use LOTRISONE cream for the prescribed treatment time, even if your symptoms get better.
    • Do not use more than 45 grams of LOTRISONE cream in 1 week.
    • Do not bandage, cover, or wrap the treated area unless your healthcare provider tells you to. Wear loose-fitting clothing if you use LOTRISONE cream in the groin area.
    • Do not use LOTRISONE cream on your face or underarms (armpits).
    • For treatment of fungal infections of the groin and body:
      • Apply a thin layer of LOTRISONE cream to the affected skin area 2 times a day for 1 week.
      • Tell your healthcare provider if the treated skin area does not improve after 1 week of treatment.
      • Do not use LOTRISONE cream for longer than 2 weeks.
    • For treatment of fungal infections of the feet:
      • Apply a thin layer of LOTRISONE cream to the affected skin area 2 times a day for 2 weeks.
      • Tell your healthcare provider if the treated skin area does not improve after 2 weeks of treatment. Do not use LOTRISONE cream longer than 4 weeks.
      • Wash your hands after applying LOTRISONE cream.
    What should I avoid while using LOTRISONE cream?
    LOTRISONE cream should not be used to treat diaper rash or redness. You should avoid applying LOTRISONE cream in the diaper area.
    What are the possible side effects of LOTRISONE cream?
    LOTRISONE cream may cause serious side effects, including:
    • LOTRISONE cream can pass through your skin. Too much LOTRISONE cream passing through your skin can cause your adrenal glands to stop working. Your healthcare provider may do blood tests to check for adrenal gland problems.
    • Vision problems. Topical corticosteroids may increase your chance of developing cataracts and glaucoma. Tell your healthcare provider if you develop blurred vision or other vision problems during treatment with LOTRISONE cream.
    The most common side effects of LOTRISONE cream include burning, tingling, rash, swelling, and infections.
    These are not all the possible side effects of LOTRISONE cream.
    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 LOTRISONE cream?
    • Store LOTRISONE cream at room temperature between 68 to 77°F (20 to 25°C).
    • Keep LOTRISONE cream and all medicines out of the reach of children.
    General information about the safe and effective use of LOTRISONE cream.
    Medicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet. Do not use LOTRISONE cream for a condition for which it was not prescribed. Do not give LOTRISONE cream 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 LOTRISONE cream that is written for health professionals.
    What are the ingredients in LOTRISONE cream?
    Active ingredients: clotrimazole and betamethasone dipropionate
    Inactive ingredients: benzyl alcohol as a preservative, ceteareth-30, cetyl alcohol plus stearyl alcohol, mineral oil, phosphoric acid, propylene glycol, purified water, sodium phosphate monobasic monohydrate, and white petrolatum
    Distributed by: Merck Sharp & Dohme Corp., a subsidiary of
    MERCK & CO., INC., Whitehouse Station, NJ 08889, USA
    For patent information: www.merck.com/product/patent/home.html
    Copyright © 1983-2019 Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.
    All rights reserved.

    usppi-mk5335A-cr-1906r005

  • PRINCIPAL DISPLAY PANEL - 15 g Tube Box

    NDC: 0085-0924-01

    15 g

    Lotrisone®
    (clotrimazole and
    betamethasone
    dipropionate)

    cream,
    1%/0.05%

    FOR TOPICAL USE ONLY,
    NOT FOR OPHTHALMIC,
    ORAL, OR INTRAVAGINAL
    USE, NOT RECOMMENDED
    FOR PATIENTS UNDER
    THE AGE OF 17 YEARS AND
    NOT RECOMMENDED FOR
    DIAPER DERMATITIS.

    Rx only

    PRINCIPAL DISPLAY PANEL - 15 g Tube Box
  • INGREDIENTS AND APPEARANCE
    LOTRISONE 
    clotrimazole and betamethasone dipropionate cream
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 0085-0924
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Clotrimazole (UNII: G07GZ97H65) (Clotrimazole - UNII:G07GZ97H65) Clotrimazole10 mg  in 1 g
    Betamethasone dipropionate (UNII: 826Y60901U) (Betamethasone - UNII:9842X06Q6M) Betamethasone0.5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    mineral oil (UNII: T5L8T28FGP)  
    petrolatum (UNII: 4T6H12BN9U)  
    cetyl alcohol (UNII: 936JST6JCN)  
    stearyl alcohol (UNII: 2KR89I4H1Y)  
    ceteareth-30 (UNII: 1R9DCZ5FOX)  
    propylene glycol (UNII: 6DC9Q167V3)  
    sodium phosphate, monobasic, monohydrate (UNII: 593YOG76RN)  
    phosphoric acid (UNII: E4GA8884NN)  
    benzyl alcohol (UNII: LKG8494WBH)  
    sodium hydroxide (UNII: 55X04QC32I)  
    Product Characteristics
    ColorWHITE (white to off-white) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 0085-0924-011 in 1 BOX07/10/1984
    115 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC: 0085-0924-021 in 1 BOX07/10/1984
    245 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA01882707/10/1984
    Labeler - Merck Sharp & Dohme Corp. (001317601)

    • Trademark Results [Lotrisone]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    LOTRISONE
    LOTRISONE
    73377500 1252707 Live/Registered
    Schering Corporation
    1982-07-30
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