Tridesilon Cream

DESONIDE 0.05% TOPICAL HUMAN PRESCRIPTION DRUG

Tridesilon Cream is an FDA drug label for the active ingredient DESONIDE 0.05% manufactured by Encore Dermatology Inc administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20160421.

Generic name
DESONIDE 0.05%
Manufacturer
Encore Dermatology Inc
Product type
HUMAN PRESCRIPTION DRUG
Route
TOPICAL
Dosage form
N/A
NDC
69482-600
Application
NDA017010
Label effective
20160421

About this product

Tridesilon Cream is an FDA-registered drug product whose active ingredient is DESONIDE 0.05%. It is labelled by Encore Dermatology Inc taken by topical and marketed as a human prescription drug product. Identifiers on file: NDC 69482-600, application NDA017010, label effective 20160421. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Dosage & Administration

Dosage & Administration Section Dosage & Administration

Frequently asked questions

What is Tridesilon Cream used for?
No indications section is present in the FDA label on file for this product. Consult the prescribing information supplied with the medicine or ask a pharmacist.

Who makes Tridesilon Cream?
Encore Dermatology Inc is the labeler of record for Tridesilon Cream.

What form does Tridesilon Cream come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Tridesilon Cream prescription or over-the-counter?
The FDA label for this product is recorded as human prescription drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Has Tridesilon Cream been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.