Product NDC: | 50804-183 |
Proprietary Name: | Complete Menstrual Relief |
Non Proprietary Name: | Acetaminophen, Caffeine, Pyrilamine maleate |
Active Ingredient(s): | 500; 60; 15 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Caffeine, Pyrilamine maleate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50804-183 |
Labeler Name: | Geiss, Destin & Dunn, Inc (Goodsense) |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120116 |
Package NDC: | 50804-183-24 |
Package Description: | 2 BLISTER PACK in 1 BOX (50804-183-24) > 12 TABLET in 1 BLISTER PACK |
NDC Code | 50804-183-24 |
Proprietary Name | Complete Menstrual Relief |
Package Description | 2 BLISTER PACK in 1 BOX (50804-183-24) > 12 TABLET in 1 BLISTER PACK |
Product NDC | 50804-183 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Caffeine, Pyrilamine maleate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20120116 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Geiss, Destin & Dunn, Inc (Goodsense) |
Substance Name | ACETAMINOPHEN; CAFFEINE; PYRILAMINE MALEATE |
Strength Number | 500; 60; 15 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |