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Backache Relief
Backache Relief - 59779-338-08 - (Magnesium Salicylate)
Drug Information of Backache Relief
| Product NDC: | 59779-338 |
| Proprietary Name: | Backache Relief |
| Non Proprietary Name: | Magnesium Salicylate |
| Active Ingredient(s): | 580 mg/1 & nbsp; Magnesium Salicylate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Backache Relief
| Product NDC: | 59779-338 |
| Labeler Name: | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19981107 |
Package Information of Backache Relief
| Package NDC: | 59779-338-08 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (59779-338-08) > 24 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Backache Relief
| NDC Code | 59779-338-08 |
| Proprietary Name | Backache Relief |
| Package Description | 1 BLISTER PACK in 1 CARTON (59779-338-08) > 24 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 59779-338 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Magnesium Salicylate |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19981107 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
| Substance Name | MAGNESIUM SALICYLATE |
| Strength Number | 580 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
