| Product NDC: | 55316-602 |
| Proprietary Name: | epsom salt |
| Non Proprietary Name: | Magnesium Sulfate |
| Active Ingredient(s): | 1 g/g & nbsp; Magnesium Sulfate |
| Administration Route(s): | ORAL; TOPICAL |
| Dosage Form(s): | GRANULE, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55316-602 |
| Labeler Name: | DZA Brands, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080227 |
| Package NDC: | 55316-602-07 |
| Package Description: | 1814 g in 1 POUCH (55316-602-07) |
| NDC Code | 55316-602-07 |
| Proprietary Name | epsom salt |
| Package Description | 1814 g in 1 POUCH (55316-602-07) |
| Product NDC | 55316-602 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Magnesium Sulfate |
| Dosage Form Name | GRANULE, FOR SOLUTION |
| Route Name | ORAL; TOPICAL |
| Start Marketing Date | 20080227 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | DZA Brands, LLC |
| Substance Name | MAGNESIUM SULFATE |
| Strength Number | 1 |
| Strength Unit | g/g |
| Pharmaceutical Classes |