Alka-Seltzer Plus Maximum Strength Day and Night Cold and Flu 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 | 0280-0040_b13d5132-cb92-3cf6-e053-2a95a90aa47c |
| NDC | 0280-0040 |
| Product Type | Human Otc Drug |
| Proprietary Name | Alka-Seltzer Plus Maximum Strength Day and Night Cold and Flu |
| Generic Name | Dextromethorphan Hydrobromide, Acetaminophen, Phenylephrine Hydrochloride, Doxylamine Succinate |
| Dosage Form | Kit |
| Route of Administration | ORAL |
| Marketing Start Date | 2020-10-26 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Labeler Name | Bayer HealthCare LLC. |
| Active Ingredient Strength | 0 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
| Marketing Start Date | 2020-10-26 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0280-0040 | Alka-Seltzer Plus Maximum Strength Day and Night Cold and Flu | dextromethorphan hydrobromide, acetaminophen, phenylephrine hydrochloride, doxylamine succinate |
| 0280-1580 | Alka-Seltzer Plus Maximum Strength Day and Night Cold and Flu | Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, Phenylephrine hydrochloride |
| 0280-1581 | Alka-Seltzer Plus Maximum Strength Day and Night Cold and Flu | Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, Phenylephrine hydrochloride |