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Derma-Smoothe/FS - 54868-5351-0 - (fluocinolone acetonide)

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Drug Information of Derma-Smoothe/FS

Product NDC: 54868-5351
Proprietary Name: Derma-Smoothe/FS
Non Proprietary Name: fluocinolone acetonide
Active Ingredient(s): .11    mg/mL & nbsp;   fluocinolone acetonide
Administration Route(s): TOPICAL
Dosage Form(s): OIL
Coding System: National Drug Codes(NDC)

Labeler Information of Derma-Smoothe/FS

Product NDC: 54868-5351
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019452
Marketing Category: NDA
Start Marketing Date: 20090903

Package Information of Derma-Smoothe/FS

Package NDC: 54868-5351-0
Package Description: 1 BOTTLE in 1 CARTON (54868-5351-0) > 118.28 mL in 1 BOTTLE

NDC Information of Derma-Smoothe/FS

NDC Code 54868-5351-0
Proprietary Name Derma-Smoothe/FS
Package Description 1 BOTTLE in 1 CARTON (54868-5351-0) > 118.28 mL in 1 BOTTLE
Product NDC 54868-5351
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluocinolone acetonide
Dosage Form Name OIL
Route Name TOPICAL
Start Marketing Date 20090903
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name FLUOCINOLONE ACETONIDE
Strength Number .11
Strength Unit mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Derma-Smoothe/FS


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