| 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 |