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 | 0280-0086_dda30b5f-bc44-57e7-e053-2995a90af709 |
NDC | 0280-0086 |
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 | 2022-04-27 |
Marketing Category | OTC MONOGRAPH FINAL / |
Application Number | part341 |
Labeler Name | Bayer HealthCare LLC. |
Active Ingredient Strength | 0 |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |
Marketing Start Date | 2022-04-29 |
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 |