Alka-Seltzer Plus Severe Cold PowerFast Fizz Day and Night is a Oral Kit in the Human Otc Drug category. It is labeled and distributed by Bayer Healthcare Llc.. The primary component is .
| Product ID | 0280-0069_c46e638b-189d-2269-e053-2995a90af8b1 |
| NDC | 0280-0069 |
| Product Type | Human Otc Drug |
| Proprietary Name | Alka-Seltzer Plus Severe Cold PowerFast Fizz Day and Night |
| Generic Name | Aspirin, Dextromethorphan Hydrobromide, Phenylephrine Bitartrate |
| Dosage Form | Kit |
| Route of Administration | ORAL |
| Marketing Start Date | 2021-08-05 |
| Marketing Category | OTC MONOGRAPH FINAL / |
| Application Number | part341 |
| Labeler Name | Bayer HealthCare LLC. |
| Active Ingredient Strength | 0 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |
| Marketing Start Date | 2021-08-05 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0280-0069 | Alka-Seltzer Plus Severe Cold PowerFast Fizz Day and Night | aspirin, dextromethorphan hydrobromide, phenylephrine bitartrate |
| 0280-0086 | Alka-Seltzer Plus Severe Cold PowerFast Fizz Day and Night | aspirin, dextromethorphan hydrobromide, phenylephrine bitartrate |
| 71992-154 | ALKA SELTZER PLUS Cold Day and Night Effervescent | ASPIRIN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE BITARTRATE |
| 0280-1540 | Alka-Seltzer Plus Multi-Symptom Cold Day and Night | Aspirin, Dextromethorphan hydrobromide, Phenylephrine bitartrate |