Home > National Drug Code (NDC) > Treatment 101

Treatment 101 - 51439-004-01 - (Sulphur)

Alphabetical Index


Drug Information of Treatment 101

Product NDC: 51439-004
Proprietary Name: Treatment 101
Non Proprietary Name: Sulphur
Active Ingredient(s): .003    mg/.06mg & nbsp;   Sulphur
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Treatment 101

Product NDC: 51439-004
Labeler Name: CarePluss Pharma S.A. de C.V.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333D
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120806

Package Information of Treatment 101

Package NDC: 51439-004-01
Package Description: .06 mg in 1 BOTTLE (51439-004-01)

NDC Information of Treatment 101

NDC Code 51439-004-01
Proprietary Name Treatment 101
Package Description .06 mg in 1 BOTTLE (51439-004-01)
Product NDC 51439-004
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Sulphur
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20120806
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name CarePluss Pharma S.A. de C.V.
Substance Name SULFUR
Strength Number .003
Strength Unit mg/.06mg
Pharmaceutical Classes

Complete Information of Treatment 101


General Information