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Desonide - Medication Information

Product NDC Code 70771-1381
Drug Name

Desonide

Type Generic
Pharm Class Corticosteroid Hormone Receptor Agonists [MoA],
Corticosteroid [EPC]
Active Ingredients
Desonide .5 mg/g
Route TOPICAL
Dosage Form CREAM
RxCUI drug identifier 349351
Application Number ANDA210198
Labeler Name Zydus Lifesciences Limited
Packages
Package NDC Code Description
70771-1381-1 1 tube in 1 carton (70771-1381-1) / 15 g in 1 tube
70771-1381-3 1 tube in 1 carton (70771-1381-3) / 60 g in 1 tube
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Spl product data elements

Usually a list of ingredients in a drug product.
Desonide Desonide DESONIDE DESONIDE ALUMINUM SULFATE CALCIUM ACETATE CETOSTEARYL ALCOHOL GLYCERIN ICODEXTRIN LIGHT MINERAL OIL METHYLPARABEN PETROLATUM SODIUM LAURYL SULFATE WATER YELLOW WAX WHITE TO OFF-WHITE

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 70771-1381-1 Desonide cream, 0.05% 15 g Rx only Desonide Cream Desonide Cream

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API