TRI-LUMA - 0299-5950-30 - (fluocinolone acetonide, hydroquinone, and tretinoin)

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Drug Information of TRI-LUMA

Product NDC: 0299-5950
Proprietary Name: TRI-LUMA
Non Proprietary Name: fluocinolone acetonide, hydroquinone, and tretinoin
Active Ingredient(s): .1; 40; .5    mg/g; mg/g; mg/g & nbsp;   fluocinolone acetonide, hydroquinone, and tretinoin
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of TRI-LUMA

Product NDC: 0299-5950
Labeler Name: Galderma Laboratories, L.P.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021112
Marketing Category: NDA
Start Marketing Date: 20020118

Package Information of TRI-LUMA

Package NDC: 0299-5950-30
Package Description: 30 g in 1 TUBE (0299-5950-30)

NDC Information of TRI-LUMA

NDC Code 0299-5950-30
Proprietary Name TRI-LUMA
Package Description 30 g in 1 TUBE (0299-5950-30)
Product NDC 0299-5950
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluocinolone acetonide, hydroquinone, and tretinoin
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20020118
Marketing Category Name NDA
Labeler Name Galderma Laboratories, L.P.
Substance Name FLUOCINOLONE ACETONIDE; HYDROQUINONE; TRETINOIN
Strength Number .1; 40; .5
Strength Unit mg/g; mg/g; mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Depigmenting Activity [PE],Melanin Synthesis Inhibitor [EPC],Melanin Synthesis Inhibitors [MoA],Retinoid [EPC],Retinoids [Chemical/Ingredient]

Complete Information of TRI-LUMA


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