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SULPHUR
SULPHUR - 10191-1578-2 - (SULFUR)
Drug Information of SULPHUR
| Product NDC: | 10191-1578 |
| Proprietary Name: | SULPHUR |
| Non Proprietary Name: | SULFUR |
| Active Ingredient(s): | 6 [hp_X]/1 & nbsp; SULFUR |
| Administration Route(s): | SUBLINGUAL |
| Dosage Form(s): | PELLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SULPHUR
| Product NDC: | 10191-1578 |
| Labeler Name: | REMEDY MAKERS |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 19981208 |
Package Information of SULPHUR
| Package NDC: | 10191-1578-2 |
| Package Description: | 137 PELLET in 1 VIAL, GLASS (10191-1578-2) |
NDC Information of SULPHUR
| NDC Code | 10191-1578-2 |
| Proprietary Name | SULPHUR |
| Package Description | 137 PELLET in 1 VIAL, GLASS (10191-1578-2) |
| Product NDC | 10191-1578 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SULFUR |
| Dosage Form Name | PELLET |
| Route Name | SUBLINGUAL |
| Start Marketing Date | 19981208 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | REMEDY MAKERS |
| Substance Name | SULFUR |
| Strength Number | 6 |
| Strength Unit | [hp_X]/1 |
| Pharmaceutical Classes |
