Desoximetasone


E. Fougera & Co. A Division Of Fougera Pharmaceuticals Inc.
Human Prescription Drug
NDC 0168-0180
Desoximetasone is a human prescription drug labeled by 'E. Fougera & Co. A Division Of Fougera Pharmaceuticals Inc.'. National Drug Code (NDC) number for Desoximetasone is 0168-0180. This drug is available in dosage form of Cream. The names of the active, medicinal ingredients in Desoximetasone drug includes Desoximetasone - 2.5 mg/g . The currest status of Desoximetasone drug is Active.

Drug Information:

Drug NDC: 0168-0180
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name: Desoximetasone
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type: Human Prescription Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name: Desoximetasone
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: E. Fougera & Co. A Division Of Fougera Pharmaceuticals Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Cream
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status: Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:DESOXIMETASONE - 2.5 mg/g
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:TOPICAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Marketing Category: ANDA
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Marketing Start Date: 29 Jun, 2010
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 22 Dec, 2025
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Application Number: ANDA078369
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
Listing Expiration Date: 31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Manufacturer Name:E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:197574
The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms.
Original Packager:Yes
Whether or not the drug has been repackaged for distribution.
NUI:N0000175576
N0000175450
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:4E07GXB7AU
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class MOA:Corticosteroid Hormone Receptor Agonists [MoA]
Mechanism of action of the drug—molecular, subcellular, or cellular functional activity—of the drug’s established pharmacologic class. Takes the form of the mechanism of action, followed by `[MoA]` (such as `Calcium Channel Antagonists [MoA]` or `Tumor Necrosis Factor Receptor Blocking Activity [MoA]`.
Pharmacologic Class EPC:Corticosteroid [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class:Corticosteroid Hormone Receptor Agonists [MoA]
Corticosteroid [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
0168-0180-151 TUBE in 1 CARTON (0168-0180-15) / 15 g in 1 TUBE29 Jun, 2010N/ANo
0168-0180-601 TUBE in 1 CARTON (0168-0180-60) / 60 g in 1 TUBE29 Jun, 2010N/ANo
0168-0180-991 TUBE in 1 CARTON (0168-0180-99) / 100 g in 1 TUBE29 Jun, 2010N/ANo
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Product Elements:

Desoximetasone desoximetasone desoximetasone desoximetasone petrolatum water isopropyl myristate lanolin alcohols mineral oil cetostearyl alcohol

Indications and Usage:

Indications and usage: desoximetasone cream usp 0.25% is indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.

Warnings:

Warnings: desoximetasone cream usp 0.25% is not for ophthalmic use. keep out of reach of children.

General Precautions:

General: systemic absorption of topical corticosteroids can produce reversible hypothalamic-pituitary-adrenal (hpa) axis suppression with the potential for clinical glucocorticosteroid insufficiency. this may occur during treatment or upon withdrawal of the topical corticosteroid. because of the potential for systemic absorption, use of topical corticosteroids may require that patients be periodically evaluated for hpa axis suppression. factors that predispose a patient using a topical corticosteroid to hpa axis suppression include the use of more potent steroids, use over large surface areas, use over prolonged periods, use under occlusion, use on an altered skin barrier, and use in patients with liver failure. an acth stimulation test may be helpful in evaluating patients for hpa axis suppression. if hpa axis suppression is documented, an attempt should be made to gradually withdraw the drug, to reduce the frequency of application, or to substitute a less potent steroid. manifestatio
ns of adrenal insufficiency may require supplemental systemic corticosteroids. recovery of hpa axis function is generally prompt and complete upon discontinuation of topical corticosteroids. cushing's syndrome, hyperglycemia, and unmasking of latent diabetes mellitus can also result from systemic absorption of topical corticosteroids. use of more than one corticosteroid-containing product at the same time may increase the total systemic corticosteroid exposure. pediatric patients may be more susceptible to systemic toxicity from use of topical corticosteroids. local adverse reactions with topical corticosteroids: local adverse reactions may be more likely to occur with occlusive use, prolonged use or use of higher potency corticosteroids. reactions may include atrophy, striae, telangiectasias, burning, itching, irritation, dryness, folliculitis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, secondary infection, and milaria. some local adverse reactions may be irreversible. allergic contact dermatitis with topical corticosteroids: allergic contact dermatitis to any component of topical corticosteroids is usually diagnosed by a failure to heal rather than a clinical exacerbation. clinical diagnosis of allergic contact dermatitis can be confirmed by patch testing. concomitant skin infections: concomitant skin infections should be treated with an appropriate antimicrobial agent. if infection persists, desoximetasone cream usp 0.25% should be discontinued until the infection has been adequately treated.

Dosage and Administration:

Dosage and administration: apply a thin film of desoximetasone cream usp 0.25% to the affected skin areas twice daily. rub in gently.

Contraindications:

Contraindications: topical steroids are contraindicated in those patients with a history of hypersensitivity to any of the components of the preparation.

Adverse Reactions:

Adverse reactions: the following local adverse reactions are reported infrequently with topical corticosteroids, but may occur more frequently with the use of occlusive dressings. these reactions are listed in an approximate decreasing order of occurrence: burning perioral dermatitis itching allergic contact dermatitis irritation maceration of the skin dryness secondary infections folliculitis skin atrophy hypertrichosis striae acneiform eruptions miliaria hypopigmentation in controlled clinical studies the incidence of adverse reactions was low (0.8%) for desoximetasone cream 0.25% and included burning, folliculitis, and folliculo-pustular lesions.

Adverse Reactions Table:

Burning Perioral dermatitis
Itching Allergic contact dermatitis
Irritation Maceration of the skin
Dryness Secondary infections
Folliculitis Skin atrophy
Hypertrichosis Striae
Acneiform eruptions Miliaria
Hypopigmentation

Pediatric Use:

Pediatric use: pediatric patients may demonstrate greater susceptibility to topical corticosteroid-induced hpa axis suppression and cushing's syndrome than mature patients because of a larger skin surface area to body weight ratio. hpa axis suppression, cushing's syndrome, and intracranial hypertension have been reported in pediatric patients receiving topical corticosteroids. manifestations of adrenal suppression in pediatric patients include linear growth retardation, delayed weight gain, low plasma cortisol levels, and absence of response to acth stimulation. manifestations of intracranial hypertension include bulging fontanelles, headaches, and bilateral papilledema. administration of topical corticosteroids to pediatric patients should be limited to the least amount compatible with an effective therapeutic regimen. chronic corticosteroid therapy may interfere with the growth and development of pediatric patients.

Overdosage:

Overdosage: topically applied corticosteroids can be absorbed in sufficient amounts to produce systemic effects (see precautions ).

Description:

Description: desoximetasone cream usp 0.25% contains the active synthetic corticosteroid desoximetasone. the topical corticosteroids constitute a class of primarily synthetic steroids used as anti-inflammatory and antipruritic agents. each gram of desoximetasone cream usp 0.25% contains 2.5 mg of desoximetasone in an emollient cream base consisting of white petrolatum, purified water, isopropyl myristate, lanolin alcohols, mineral oil, and cetostearyl alcohol. the chemical name of desoximetasone is: pregna-1,4-diene-3,20-dione,9-fluoro-11,21-dihydroxy-16-methyl-,(11β,16α)-. desoximetasone has the molecular formula c 22 h 29 fo 4 and the molecular weight of 376.47. the cas registry number is 382-67-2. the structural formula is: structural formula

Clinical Pharmacology:

Clinical pharmacology: topical corticosteroids share anti-inflammatory, anti-pruritic and vasoconstrictive actions. the mechanism of anti-inflammatory activity of the topical corticosteroids is unclear. various laboratory methods, including vasoconstrictor assays, are used to compare and predict potencies and/or clinical efficacies of the topical corticosteroids. there is some evidence to suggest that a recognizable correlation exists between vasoconstrictor potency and therapeutic efficacy in man. pharmacokinetics: 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 increase percutaneous absorption. occlusive dressings substantially increase the percutaneous absorption of topical corticosteroids. thus, occlusive dressings may
be a valuable therapeutic adjunct for treatment of resistant dermatoses. once absorbed through the skin, topical corticosteroids are handled through pharmacokinetic pathways 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. pharmacokinetic studies in men with desoximetasone cream usp 0.25% with tagged desoximetasone showed a total of 5.2% ± 2.9% excretion in urine (4.1% ± 2.3%) and feces (1.1% ± 0.6%) and no detectable level (limit of sensitivity: 0.005 ug/ml) in the blood when it was applied topically on the back followed by occlusion for 24 hours. seven days after application, no further radioactivity was detected in urine or feces. the half-life of the material was 15 ± 2 hours (for urine) and 17 ± 2 hours (for feces) between the third and fifth trial day. studies with other similarly structured steroids have shown that predominant metabolite reaction occurs through conjugation to form the glucuronide and sulfate ester.

Carcinogenesis and Mutagenesis and Impairment of Fertility:

Carcinogenesis, mutagenesis, impairment of fertility: long-term animal studies have not been performed to evaluate the carcinogenic potential or the effect on fertility of desoximetasone. desoximetasone was nonmutagenic in the ames test.

How Supplied:

How supplied: desoximetasone cream usp 0.25% is supplied as follows: ndc 0168-0180-15 15 gram tube ndc 0168-0180-60 60 gram tube ndc 0168-0180-99 100 gram tube store at 20° to 25°c (68° to 77°f), excursions permitted to 15° to 30°c (59° to 86°f). [see usp controlled room temperature] e. fougera & co. a division of fougera pharmaceuticals inc. melville, new york 11747 i2180c r10/12 #115

Information for Patients:

Information for patients: patients using topical corticosteroids should receive the following information and instructions: 1. this medication is to be used as directed by the physician. it is for external use only. avoid contact with the eyes. 2. patients should be advised not to use this medication for any disorder other than for which it was prescribed. 3. the treated skin area should not be bandaged or otherwise covered or wrapped as to be occlusive unless directed by the physician. 4. patients should report any signs of local adverse reactions especially under occlusive dressing. 5. other corticosteroid-containing products should not be used with desoximetasone cream usp 0.25% without first consulting with the physician. as with other corticosteroids, therapy should be discontinued when control is achieved. if no improvement is seen within 4 weeks, contact the physician.

Package Label Principal Display Panel:

Package label – principal display panel – 15g container ndc 0168-0180-15 fougera ® desoximetasone cream usp 0.25% rx only for external use only. not for oral, ophthalmic, or intravaginal use. warning: keep out of reach of children. net wt 15 grams package label – principal display panel – 15g container

Package label – principal display panel – 15g carton ndc 0168-0180-15 rx only fougera ® desoximetasone cream usp 0.25% for external use only. not for oral, ophthalmic, or intravaginal use. warning: keep out of reach of children. net wt 15 grams package label – principal display panel – 15g carton


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