Product NDC: | 59779-583 |
Proprietary Name: | Allergy and Cold |
Non Proprietary Name: | Acetaminophen, Diphenhydramine HCl and Phenylephrine HCl |
Active Ingredient(s): | 325; 12.5; 5 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Diphenhydramine HCl and Phenylephrine HCl |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, GELATIN COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59779-583 |
Labeler Name: | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090710 |
Package NDC: | 59779-583-08 |
Package Description: | 1 BLISTER PACK in 1 CARTON (59779-583-08) > 24 CAPSULE, GELATIN COATED in 1 BLISTER PACK |
NDC Code | 59779-583-08 |
Proprietary Name | Allergy and Cold |
Package Description | 1 BLISTER PACK in 1 CARTON (59779-583-08) > 24 CAPSULE, GELATIN COATED in 1 BLISTER PACK |
Product NDC | 59779-583 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Diphenhydramine HCl and Phenylephrine HCl |
Dosage Form Name | CAPSULE, GELATIN COATED |
Route Name | ORAL |
Start Marketing Date | 20090710 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 325; 12.5; 5 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |