ALKA SELTZER PLUS Cold Day and Night Effervescent is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Sincronia Logistica, S.a. De C.v.. The primary component is Aspirin; Dextromethorphan Hydrobromide; Phenylephrine Bitartrate.
| Product ID | 71992-154_6ada0b51-72a3-279d-e053-2a91aa0a160c |
| NDC | 71992-154 |
| Product Type | Human Otc Drug |
| Proprietary Name | ALKA SELTZER PLUS Cold Day and Night Effervescent |
| Generic Name | Aspirin, Dextromethorphan Hydrobromide, Phenylephrine Bitartrate |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2018-07-02 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Labeler Name | Sincronia Logistica, S.A. de C.V. |
| Substance Name | ASPIRIN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE BITARTRATE |
| Active Ingredient Strength | 325 mg/1; mg/1; mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2018-07-02 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-07-02 |
| Ingredient | Strength |
|---|---|
| ASPIRIN | 325 mg/1 |
| SPL SET ID: | c478df69-823a-4112-8f44-323249a9f38f |
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| Pharm Class PE | |
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| NUI Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 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 |
| 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 |