| Product NDC: | 0280-1158 |
| Proprietary Name: | Alka-Seltzer Plus Night Severe Cold, Cough And Flu |
| Non Proprietary Name: | Acetaminophen, Diphenhydramine hydrochloride, and Phenylephrine hydrochloride |
| Active Ingredient(s): | 650; 25; 10 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Diphenhydramine hydrochloride, and Phenylephrine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0280-1158 |
| Labeler Name: | Bayer HealthCare LLC - Consumer Care |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120731 |
| Package NDC: | 0280-1158-06 |
| Package Description: | 6 PACKET in 1 CARTON (0280-1158-06) > 1 POWDER in 1 PACKET |
| NDC Code | 0280-1158-06 |
| Proprietary Name | Alka-Seltzer Plus Night Severe Cold, Cough And Flu |
| Package Description | 6 PACKET in 1 CARTON (0280-1158-06) > 1 POWDER in 1 PACKET |
| Product NDC | 0280-1158 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Diphenhydramine hydrochloride, and Phenylephrine hydrochloride |
| Dosage Form Name | POWDER |
| Route Name | ORAL |
| Start Marketing Date | 20120731 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Bayer HealthCare LLC - Consumer Care |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 650; 25; 10 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |