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Alka-Seltzer Plus Day Severe Cold, Cough And Flu
Alka-Seltzer Plus Day Severe Cold, Cough And Flu - 0280-1155-06 - (Acetaminophen, Dextromethorphan hydrobromide, and Phenylephrine hydrochloride)
Drug Information of Alka-Seltzer Plus Day Severe Cold, Cough And Flu
| Product NDC: | 0280-1155 |
| Proprietary Name: | Alka-Seltzer Plus Day Severe Cold, Cough And Flu |
| Non Proprietary Name: | Acetaminophen, Dextromethorphan hydrobromide, and Phenylephrine hydrochloride |
| Active Ingredient(s): | 650; 20; 10 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Dextromethorphan hydrobromide, and Phenylephrine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Alka-Seltzer Plus Day Severe Cold, Cough And Flu
| Product NDC: | 0280-1155 |
| 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 Information of Alka-Seltzer Plus Day Severe Cold, Cough And Flu
| Package NDC: | 0280-1155-06 |
| Package Description: | 6 PACKET in 1 CARTON (0280-1155-06) > 1 POWDER in 1 PACKET |
NDC Information of Alka-Seltzer Plus Day Severe Cold, Cough And Flu
| NDC Code | 0280-1155-06 |
| Proprietary Name | Alka-Seltzer Plus Day Severe Cold, Cough And Flu |
| Package Description | 6 PACKET in 1 CARTON (0280-1155-06) > 1 POWDER in 1 PACKET |
| Product NDC | 0280-1155 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Dextromethorphan hydrobromide, 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; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 650; 20; 10 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
