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BACK RELIEF
BACK RELIEF - 0498-2101-10 - (ACETAMINOPHEN, MAGNESIUM SALICYLATE)
Drug Information of BACK RELIEF
| Product NDC: | 0498-2101 |
| Proprietary Name: | BACK RELIEF |
| Non Proprietary Name: | ACETAMINOPHEN, MAGNESIUM SALICYLATE |
| Active Ingredient(s): | 200; 200 mg/1; mg/1 & nbsp; ACETAMINOPHEN, MAGNESIUM SALICYLATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BACK RELIEF
| Product NDC: | 0498-2101 |
| Labeler Name: | North Safety Products LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130514 |
Package Information of BACK RELIEF
| Package NDC: | 0498-2101-10 |
| Package Description: | 50 PACKET in 1 CARTON (0498-2101-10) > 2 TABLET in 1 PACKET (0498-2101-01) |
NDC Information of BACK RELIEF
| NDC Code | 0498-2101-10 |
| Proprietary Name | BACK RELIEF |
| Package Description | 50 PACKET in 1 CARTON (0498-2101-10) > 2 TABLET in 1 PACKET (0498-2101-01) |
| Product NDC | 0498-2101 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ACETAMINOPHEN, MAGNESIUM SALICYLATE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130514 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | North Safety Products LLC |
| Substance Name | ACETAMINOPHEN; MAGNESIUM SALICYLATE |
| Strength Number | 200; 200 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
