Drugplain

ALKA SELTZER PLUS Cold Day and Night Effervescent 325 mg/1

ASPIRIN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE BITARTRATE · TABLET · Sincronia Logistica, S.A. de C.V.

No Recall History
Plain English

ALKA SELTZER PLUS Cold Day and Night Effervescent is a tablet containing aspirin, dextromethorphan hydrobromide, phenylephrine bitartrate at 325 mg/1, taken oral. Manufactured by Sincronia Logistica, S.A. de C.V..

Key Facts

Brand Name
ALKA SELTZER PLUS Cold Day and Night Effervescent
Generic Name
ASPIRIN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE BITARTRATE
NDC Code (Product)
71992-154
Manufacturer
Sincronia Logistica, S.A. de C.V.
Strength
325 mg/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
Application #
M012
Drug Class
Nonsteroidal Anti-inflammatory Drug [EPC]; Platelet Aggregation Inhibitor [EPC]
Marketing Start
07/02/2018

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

fatigue1 reports
haematochezia1 reports
nausea1 reports
pyrexia1 reports

Frequently Asked Questions

What is ALKA SELTZER PLUS Cold Day and Night Effervescent used for?

ALKA SELTZER PLUS Cold Day and Night Effervescent contains ASPIRIN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE BITARTRATE. It is a tablet taken oral. Consult your doctor for specific uses.

Is ALKA SELTZER PLUS Cold Day and Night Effervescent a controlled substance?

ALKA SELTZER PLUS Cold Day and Night Effervescent is not classified as a controlled substance by the DEA.

What is the generic name for ALKA SELTZER PLUS Cold Day and Night Effervescent?

The generic name for ALKA SELTZER PLUS Cold Day and Night Effervescent is ASPIRIN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE BITARTRATE. There are 4 other brand versions of ASPIRIN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE BITARTRATE.

What is the NDC code for ALKA SELTZER PLUS Cold Day and Night Effervescent 325 mg/1?

The NDC (National Drug Code) for ALKA SELTZER PLUS Cold Day and Night Effervescent 325 mg/1 is 71992-154, listed by Sincronia Logistica, S.A. de C.V..

Product NDC

71992-154

Package NDC

71992-154-20

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)