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Sulfur
Sulfur - 68437-010-01 - (Sulfur)
Drug Information of Sulfur
| Product NDC: | 68437-010 |
| Proprietary Name: | Sulfur |
| Non Proprietary Name: | Sulfur |
| Active Ingredient(s): | 10 g/100g & nbsp; Sulfur |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sulfur
| Product NDC: | 68437-010 |
| Labeler Name: | GRISI Hnos, S.A DE C.V |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121201 |
Package Information of Sulfur
| Package NDC: | 68437-010-01 |
| Package Description: | 1 TUBE in 1 CARTON (68437-010-01) > 20 g in 1 TUBE (68437-010-20) |
NDC Information of Sulfur
| NDC Code | 68437-010-01 |
| Proprietary Name | Sulfur |
| Package Description | 1 TUBE in 1 CARTON (68437-010-01) > 20 g in 1 TUBE (68437-010-20) |
| Product NDC | 68437-010 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sulfur |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20121201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | GRISI Hnos, S.A DE C.V |
| Substance Name | SULFUR |
| Strength Number | 10 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
