Drugplain

Alka-Seltzer Plus Severe Cold PowerFast Fizz

aspirin, dextromethorphan hydrobromide, phenylephrine bitartrate, doxylamine succinate · KIT · Bayer HealthCare LLC.

No Recall History
Plain English

Alka-Seltzer Plus Severe Cold Powerfast Fizz is an over-the-counter combination product containing aspirin, dextromethorphan, phenylephrine, and doxylamine that works to relieve multiple cold symptoms including pain, cough, nasal congestion, and runny nose. The medication comes as a fizzy powder kit meant to be dissolved in water and taken by mouth.

Key Facts

Brand Name
Alka-Seltzer Plus Severe Cold PowerFast Fizz
Generic Name
aspirin, dextromethorphan hydrobromide, phenylephrine bitartrate, doxylamine succinate
NDC Code (Product)
0280-0025
Manufacturer
Bayer HealthCare LLC.
Dosage Form
KIT
Route
ORAL
Marketing Status
Application #
M012
Marketing Start
04/01/2020

Recall History

No Recall History

Frequently Asked Questions

What is Alka-Seltzer Plus Severe Cold PowerFast Fizz used for?

Alka-Seltzer Plus Severe Cold Powerfast Fizz is an over-the-counter combination product containing aspirin, dextromethorphan, phenylephrine, and doxylamine that works to relieve multiple cold symptoms including pain, cough, nasal congestion, and runny nose. The medication comes as a fizzy powder kit meant to be dissolved in water and taken by mouth.

Is Alka-Seltzer Plus Severe Cold PowerFast Fizz a controlled substance?

Alka-Seltzer Plus Severe Cold PowerFast Fizz is not classified as a controlled substance by the DEA.

What is the generic name for Alka-Seltzer Plus Severe Cold PowerFast Fizz?

The generic name for Alka-Seltzer Plus Severe Cold PowerFast Fizz is aspirin, dextromethorphan hydrobromide, phenylephrine bitartrate, doxylamine succinate. There are 1 other brand versions of aspirin, dextromethorphan hydrobromide, phenylephrine bitartrate, doxylamine succinate.

What is the NDC code for Alka-Seltzer Plus Severe Cold PowerFast Fizz ?

The NDC (National Drug Code) for Alka-Seltzer Plus Severe Cold PowerFast Fizz is 0280-0025, listed by Bayer HealthCare LLC..

Product NDC

0280-0025

Package NDC

0280-0025-01

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

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