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DDF Sulfur Therapeutic - 37000-701-11 - (sulfur)

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Drug Information of DDF Sulfur Therapeutic

Product NDC: 37000-701
Proprietary Name: DDF Sulfur Therapeutic
Non Proprietary Name: sulfur
Active Ingredient(s): 100    mg/g & nbsp;   sulfur
Administration Route(s): TOPICAL
Dosage Form(s): PASTE
Coding System: National Drug Codes(NDC)

Labeler Information of DDF Sulfur Therapeutic

Product NDC: 37000-701
Labeler Name: Procter & Gamble Manufacturing Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part333D
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130501

Package Information of DDF Sulfur Therapeutic

Package NDC: 37000-701-11
Package Description: 1 JAR in 1 CARTON (37000-701-11) > 113 g in 1 JAR

NDC Information of DDF Sulfur Therapeutic

NDC Code 37000-701-11
Proprietary Name DDF Sulfur Therapeutic
Package Description 1 JAR in 1 CARTON (37000-701-11) > 113 g in 1 JAR
Product NDC 37000-701
Product Type Name HUMAN OTC DRUG
Non Proprietary Name sulfur
Dosage Form Name PASTE
Route Name TOPICAL
Start Marketing Date 20130501
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Procter & Gamble Manufacturing Company
Substance Name SULFUR
Strength Number 100
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of DDF Sulfur Therapeutic


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