Amcinonide AMCINONIDE SOLUBIOMIX, LLC FDA Approved The topical corticosteroids constitute a class of primarily synthetic steroids used as anti-inflammatory and antipruritic agents. Each gram of Amcinonide Ointment USP, 0.1% contains 1 mg of the active steroid amcinonide in a specially formulated base composed of Benzyl Alcohol 2%, (wt/wt) as preservative, White Petrolatum, USP, Emulsifying Wax, and Antioxidant Blend (Propylene Glycol, Butylated Hydroxyanisole, Propyl Gallate and Citric Acid). Chemically, amcinonide is: Pregna-1,4-diene-3,20-dione,21-(acetyloxy)-16,17-[cyclopentylidenebis(oxy)]-9-fluoro-11-hydroxy-, (11β, 16α). Chemical Formula
Generic: AMCINONIDE
Mfr: SOLUBIOMIX, LLC FDA Rx Only
FunFoxMeds bottle
Substance Amcinonide
Route
TOPICAL
Applications
ANDA076065
Package NDC

Drug Facts

Composition & Profile

Strengths
0.1 % 1 mg/g 30 g
Treats Conditions
Indications And Usage Topical Corticosteroids Are Indicated For The Relief Of The Inflammatory And Pruritic Manifestations Of Corticosteroid Responsive Dermatoses

Identifiers & Packaging

Container Type BOTTLE
All Product Codes
UNII
423W026MA9
Packaging

HOW SUPPLIED: Amcinonide Cream USP, 0.1% (1 mg/g) is supplied as follows: NDC 69499-410-30; 30 gram tubes Store at 20°C to 25°C (68°F to 77°F),excursions permitted 15°C to 30°C (59°F to 86°F). [See USP Controlled Room Temperature]. DO NOT FREEZE. Manufactured for: Solubiomix, LLC Madisonville, LA 70461 Rev. 07/23; PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – 30 G TUBE NDC 69499-410-30 Solubiomix, LLC AMCINONIDE CREAM USP, 0.1% Rx only NOT FOR OPHTHALMIC USE. FOR DERMATOLOGIC USE ONLY. NET WT 30 grams PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – 60 G CONTAINER; PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – 30 G CARTON NDC 69499-410-30 Rx only Solubiomix, LLC AMCINONIDE CREAM USP, 0.1% NOT FOR OPHTHALMIC USE. FOR DERMATOLOGIC USE ONLY. NET WT 30 grams PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – 60 G CARTON

Package Descriptions
  • HOW SUPPLIED: Amcinonide Cream USP, 0.1% (1 mg/g) is supplied as follows: NDC 69499-410-30; 30 gram tubes Store at 20°C to 25°C (68°F to 77°F),excursions permitted 15°C to 30°C (59°F to 86°F). [See USP Controlled Room Temperature]. DO NOT FREEZE. Manufactured for: Solubiomix, LLC Madisonville, LA 70461 Rev. 07/23
  • PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – 30 G TUBE NDC 69499-410-30 Solubiomix, LLC AMCINONIDE CREAM USP, 0.1% Rx only NOT FOR OPHTHALMIC USE. FOR DERMATOLOGIC USE ONLY. NET WT 30 grams PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – 60 G CONTAINER
  • PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – 30 G CARTON NDC 69499-410-30 Rx only Solubiomix, LLC AMCINONIDE CREAM USP, 0.1% NOT FOR OPHTHALMIC USE. FOR DERMATOLOGIC USE ONLY. NET WT 30 grams PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – 60 G CARTON

Overview

The topical corticosteroids constitute a class of primarily synthetic steroids used as anti-inflammatory and antipruritic agents. Each gram of Amcinonide Ointment USP, 0.1% contains 1 mg of the active steroid amcinonide in a specially formulated base composed of Benzyl Alcohol 2%, (wt/wt) as preservative, White Petrolatum, USP, Emulsifying Wax, and Antioxidant Blend (Propylene Glycol, Butylated Hydroxyanisole, Propyl Gallate and Citric Acid). Chemically, amcinonide is: Pregna-1,4-diene-3,20-dione,21-(acetyloxy)-16,17-[cyclopentylidenebis(oxy)]-9-fluoro-11-hydroxy-, (11β, 16α). Chemical Formula

Indications & Usage

: Topical corticosteroids are indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.

Dosage & Administration

: Topical corticosteroids are generally applied to the affected area as a thin film from two to three times daily depending on the severity of the condition. Occlusive dressings may be a valuable therapeutic adjunct for the management of psoriasis or recalcitrant conditions. If an infection develops, the use of occlusive dressings should be discontinued and appropriate antimicrobial therapy instituted.

Warnings & Precautions
No warnings available yet.
Contraindications

: Topical corticosteroids are contraindicated in those patients with a history of hypersensitivity to any of the components of the preparation.

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, maceration of the skin, secondary infection, skin atrophy, striae and miliaria. To report SUSPECTED ADVERSE REACTIONS, contact Pharm-Olam at 1-866-511-6754 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.


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