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Fem Relief
Fem Relief - 0498-7000-50 - (Acetaminophen Pamabrom)
Drug Information of Fem Relief
| Product NDC: | 0498-7000 |
| Proprietary Name: | Fem Relief |
| Non Proprietary Name: | Acetaminophen Pamabrom |
| Active Ingredient(s): | 325; 25 mg/1; mg/1 & nbsp; Acetaminophen Pamabrom |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fem Relief
| Product NDC: | 0498-7000 |
| Labeler Name: | North Safety Products LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120215 |
Package Information of Fem Relief
| Package NDC: | 0498-7000-50 |
| Package Description: | 250 BOX in 1 BOX (0498-7000-50) > 125 BOX in 1 BOX (0498-7000-25) > 50 PACKET in 1 BOX (0498-7000-10) > 2 TABLET in 1 PACKET (0498-7000-01) |
NDC Information of Fem Relief
| NDC Code | 0498-7000-50 |
| Proprietary Name | Fem Relief |
| Package Description | 250 BOX in 1 BOX (0498-7000-50) > 125 BOX in 1 BOX (0498-7000-25) > 50 PACKET in 1 BOX (0498-7000-10) > 2 TABLET in 1 PACKET (0498-7000-01) |
| Product NDC | 0498-7000 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen Pamabrom |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120215 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | North Safety Products LLC |
| Substance Name | ACETAMINOPHEN; PAMABROM |
| Strength Number | 325; 25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
