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Valley Medical Pharmacy
630 Main Street (Store open 8.30to 5.30pm)
Brawley, CA 92227 eRx ID#0585957

1-800-322-0808/760-344-6303/FAX-760-344-6321 Toll Free Fax#855-322-0808 Store Op
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Prescription Drugs-F > Fluocinonide > Fluocinonide 0.05% Cream 1X15 gm Mfg.by: Teva Pharm USA.

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Fluocinonide 0.05% Cream 1X15 gm Mfg.by: Teva Pharm USA.

Fluocinonide 0.05% Cream 1X15 gm Mfg.by: Teva Pharm USA. This item requires a valid order from a physician licensed in the USA. Item No.:RXD1233378 NDC No.: 00093-0262-15 Category: Fluocinonide Compare to: Lidex
UPC No.: 300930262159 Mfg.Item No.:026215

$ 13.99         

Please provide us the name, address, phone #, fax #, state lic.#, name of state, dea#, and npi# of ordering physician. Please provide all information available and ask your physician to fax us the prescription at 760-344-6321 for the quantity.

Quantity:    

Compares To: Lidex-E® and Lidex® LIDEX (fluocinonide) Cream DRUG DESCRIPTION LIDEX (fluocinonide) Cream 0.05% is intended for topical administration. The active component is the corticosteroid fluocinonide, which is the 21-acetate ester of fluocinolone acetonide and has the chemical name pregna-1,4-diene-3,20-dione,21-(acetyloxy)-6,9-difluoro-11-hydroxy-16,17-[(1-methylethylidene)bis(oxy)]-,(6α,11β,16α)-. LIDEX Cream contains fluocinonide 0.5 mg/g in FAPG® cream, a specially formulated cream base consisting of citric acid, 1,2,6-hexanetriol, polyethylene glycol 8000, propylene glycol and stearyl alcohol. This white cream vehicle is greaseless, non-staining, anhydrous and completely water miscible. The base provides emollient and hydrophylic properties. In this formulation, the active ingredient is totally in solution. INDICATIONS LIDEX Cream is indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses. DOSAGE AND ADMINISTRATION LIDEX Cream is generally applied to the affected area as a thin film from two to four times daily depending on the severity of the condition. Occlusive dressings may be used for the management of psoriasis or recalcitrant conditions. If an infection develops, the use of the occlusive dressings should be discontinued and appropriate antimicrobial therapy instituted. SIDE EFFECTS 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 Itching Irritation Dryness Folliculitis Hypertrichosis Acneiform eruptions Hypopigmentation Perioral dermatitis Allergic contact dermatitis Maceration of the skin Secondary infection Skin atrophy Striae Miliaria PRECAUTIONS General Systemic absorption of topical corticosteroids has produced reversible hypothalamic-pituitary-adrenal (HPA) axis suppression, manifestations of Cushing's syndrome, hyperglycemia, and glucosuria in some patients. Conditions which augment systemic absorption include the application of the more potent steroids, use over large surface areas, prolonged use, and the addition of occlusive dressings. Therefore, patients receiving a large dose of a potent topical steroid applied to a large surface area or under an occlusive dressing should be evaluated periodically for evidence of HPA axis suppression by using the urinary free cortisol and ACTH stimulation tests. If HPA axis suppression is noted, an attempt should be made to withdraw the drug, to reduce the frequency of application, or to substitute a less potent steroid.

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