Drugplain

Flurandrenolide .5 mg/mL

Flurandrenolide · LOTION · Bryant Ranch Prepack

No Recall History
Plain English

Flurandrenolide is a lotion containing flurandrenolide at .5 mg/mL, taken topical. Manufactured by Bryant Ranch Prepack.

Key Facts

Brand Name
Flurandrenolide
Generic Name
Flurandrenolide
NDC Code (Product)
63629-8657
Manufacturer
Bryant Ranch Prepack
Strength
.5 mg/mL
Dosage Form
LOTION
Route
TOPICAL
Marketing Status
Application #
ANDA207133
Drug Class
Corticosteroid [EPC]
Marketing Start
10/06/2016

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

headache6 reports
drug ineffective5 reports
swelling face5 reports
off label use4 reports
pain4 reports
pruritus4 reports
blister3 reports
deep vein thrombosis3 reports
diarrhoea3 reports
drug ineffective for unapproved indication3 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

INDICATIONS AND USAGE Flurandrenolide Lotion USP, 0.05% is indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.

Dosage & Administration

DOSAGE AND ADMINISTRATION Shake well before using. A small quantity of Flurandrenolide Lotion USP, 0.05% should be rubbed gently into the affected area 2 or 3 times daily. Therapy should be discontinued when control is achieved. If no improvement is seen within 2 weeks, reassessment of the diagnosis may be necessary. Flurandrenolide Lotion USP, 0.05% should not be used with occlusive dressings unless directed by a physician. Tight-fitting diapers or plastic pants may constitute occlusive dressings.

Contraindications

CONTRAINDICATIONS Topical corticosteroids are contraindicated in patients with a history of hypersensitivity to any of the components of these preparations.

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 Itching Irritation Dryness Folliculitis Hypertrichosis Acneiform eruptions Hypopigmentation Perioral dermatitis Allergic contact dermatitis The following may occur more frequently with occlusive dressings: Maceration of the skin Secondary infection Skin atrophy Striae Miliaria Postmarketing Adverse Reactions The following adverse reactions have been identified during post approval use of flurandrenolide lotion. Because these 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. Skin : skin striae, hypersensitivity, skin atrophy, contact dermatitis, and skin discoloration.

Frequently Asked Questions

What is Flurandrenolide used for?

Flurandrenolide contains Flurandrenolide. It is a lotion taken topical. Consult your doctor for specific uses.

Is Flurandrenolide a controlled substance?

Flurandrenolide is not classified as a controlled substance by the DEA.

What is the generic name for Flurandrenolide?

The generic name for Flurandrenolide is Flurandrenolide. There are 3 other brand versions of Flurandrenolide.

What is the NDC code for Flurandrenolide .5 mg/mL?

The NDC (National Drug Code) for Flurandrenolide .5 mg/mL is 63629-8657, listed by Bryant Ranch Prepack.

Product NDC

63629-8657

Package NDC

63629-8657-1

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)