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