Hydrocortisone HYDROCORTISONE E. FOUGERA & CO. A DIVISION OF FOUGERA PHARMACEUTICALS INC. FDA Approved Hydrocortisone Ointment USP, 1% contains hydrocortisone [Pregn-4-ene-3,20-dione, 11,17,21-trihydroxy-, (11ß)-], with the molecular formula C 21 H 30 O 5 and molecular weight 362.47. Each gram contains 10 mg of hydrocortisone, USP in a base containing white petrolatum and mineral oil. structure
FunFoxMeds bottle
Substance Hydrocortisone
Route
TOPICAL
Applications
ANDA080692

Drug Facts

Composition & Profile

Strengths
1 % 28.35 g 453.6 g
Quantities
31 count
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
UNII
WI4X0X7BPJ
Packaging

HOW SUPPLIED Hydrocortisone Ointment USP, 1% is supplied as follows: NDC 0168-0020-31 28.35 g (1 Oz) Tubes NDC 0168-0020-16 453.6 g (1 lb) Jars Store at controlled room temperature 15° to 30°C (59° to 86°F). E. FOUGERA & CO. A division of Fougera PHARMACEUTICALS INC. Melville, New York 11747 Rev. 07/2024; PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – 1LB CONTAINER NDC 0168-0020-16 Hydrocortisone Ointment USP, 1% Rx only For External Use Only Not For Ophthalmic Use Net Wt. 453.6 g (1 lb) FOUGERA ® jar-lbl

Package Descriptions
  • HOW SUPPLIED Hydrocortisone Ointment USP, 1% is supplied as follows: NDC 0168-0020-31 28.35 g (1 Oz) Tubes NDC 0168-0020-16 453.6 g (1 lb) Jars Store at controlled room temperature 15° to 30°C (59° to 86°F). E. FOUGERA & CO. A division of Fougera PHARMACEUTICALS INC. Melville, New York 11747 Rev. 07/2024
  • PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – 1LB CONTAINER NDC 0168-0020-16 Hydrocortisone Ointment USP, 1% Rx only For External Use Only Not For Ophthalmic Use Net Wt. 453.6 g (1 lb) FOUGERA ® jar-lbl

Overview

Hydrocortisone Ointment USP, 1% contains hydrocortisone [Pregn-4-ene-3,20-dione, 11,17,21-trihydroxy-, (11ß)-], with the molecular formula C 21 H 30 O 5 and molecular weight 362.47. Each gram contains 10 mg of hydrocortisone, USP in a base containing white petrolatum and mineral oil. structure

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 three or four times a day 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 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.


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