Drugplain

Alka-Seltzer Plus Severe Cold and Flu PowerFast Fizz 250 mg/1

chlorpheniramine maleate, acetaminophen, phenylephrine hydrochloride, dextromethorphan hydrobromide · TABLET, EFFERVESCENT · Bayer HealthCare LLC.

No Recall History
Plain English

Alka-Seltzer Plus Severe Cold and Flu PowerFast Fizz is a tablet, effervescent containing chlorpheniramine maleate, acetaminophen, phenylephrine hydrochloride, dextromethorphan hydrobromide at 250 mg/1, taken oral. Manufactured by Bayer HealthCare LLC..

Key Facts

Brand Name
Alka-Seltzer Plus Severe Cold and Flu PowerFast Fizz
Generic Name
chlorpheniramine maleate, acetaminophen, phenylephrine hydrochloride, dextromethorphan hydrobromide
NDC Code (Product)
0280-0088
Manufacturer
Bayer HealthCare LLC.
Strength
250 mg/1
Dosage Form
TABLET, EFFERVESCENT
Route
ORAL
Marketing Status
Application #
M012
Marketing Start
04/05/2022

Recall History

No Recall History

Frequently Asked Questions

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

Alka-Seltzer Plus Severe Cold and Flu PowerFast Fizz contains chlorpheniramine maleate, acetaminophen, phenylephrine hydrochloride, dextromethorphan hydrobromide. It is a tablet, effervescent taken oral. Consult your doctor for specific uses.

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

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

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

The generic name for Alka-Seltzer Plus Severe Cold and Flu PowerFast Fizz is chlorpheniramine maleate, acetaminophen, phenylephrine hydrochloride, dextromethorphan hydrobromide. There are 3 other brand versions of chlorpheniramine maleate, acetaminophen, phenylephrine hydrochloride, dextromethorphan hydrobromide.

What is the NDC code for Alka-Seltzer Plus Severe Cold and Flu PowerFast Fizz 250 mg/1?

The NDC (National Drug Code) for Alka-Seltzer Plus Severe Cold and Flu PowerFast Fizz 250 mg/1 is 0280-0088, listed by Bayer HealthCare LLC..

Product NDC

0280-0088

Package NDC

0280-0088-01

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

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