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Clarifoam EF - 16781-154-06 - (SULFUR,SULFACETAMIDE SODIUM)

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Drug Information of Clarifoam EF

Product NDC: 16781-154
Proprietary Name: Clarifoam EF
Non Proprietary Name: SULFUR,SULFACETAMIDE SODIUM
Active Ingredient(s): 10; 5    g/100g; g/100g & nbsp;   SULFUR,SULFACETAMIDE SODIUM
Administration Route(s): TOPICAL
Dosage Form(s): AEROSOL, FOAM
Coding System: National Drug Codes(NDC)

Labeler Information of Clarifoam EF

Product NDC: 16781-154
Labeler Name: Onset Dermatologics LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20070601

Package Information of Clarifoam EF

Package NDC: 16781-154-06
Package Description: 5 g in 1 CAN (16781-154-06)

NDC Information of Clarifoam EF

NDC Code 16781-154-06
Proprietary Name Clarifoam EF
Package Description 5 g in 1 CAN (16781-154-06)
Product NDC 16781-154
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SULFUR,SULFACETAMIDE SODIUM
Dosage Form Name AEROSOL, FOAM
Route Name TOPICAL
Start Marketing Date 20070601
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Onset Dermatologics LLC
Substance Name SULFACETAMIDE SODIUM; SULFUR
Strength Number 10; 5
Strength Unit g/100g; g/100g
Pharmaceutical Classes Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient]

Complete Information of Clarifoam EF


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