Drugplain

Alka-Seltzer Plus Maximum Strength Sinus Congestion and Pain PowerFast Fizz 325 mg/1

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

No Recall History
Plain English

Alka-Seltzer Plus Maximum Strength Sinus Congestion and Pain PowerFast Fizz is a tablet, effervescent containing chlorpheniramine maleate, dextromethorphan hydrobromide, acetaminophen, phenylephrine hydrochloride at 325 mg/1, taken oral. Manufactured by Bayer HealthCare LLC..

Key Facts

Brand Name
Alka-Seltzer Plus Maximum Strength Sinus Congestion and Pain PowerFast Fizz
Generic Name
chlorpheniramine maleate, dextromethorphan hydrobromide, acetaminophen, phenylephrine hydrochloride
NDC Code (Product)
0280-0055
Manufacturer
Bayer HealthCare LLC.
Strength
325 mg/1
Dosage Form
TABLET, EFFERVESCENT
Route
ORAL
Marketing Status
Application #
M012
Marketing Start
06/15/2021

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses temporarily relieves these symptoms due to a cold or flu: minor aches and pains headache cough sore throat runny nose sneezing nasal congestion · sinus temporarily reduces fever

Dosage & Administration

Directions do not take more than the recommended dose adults and children 12 years and over: take 2 tablets fully dissolved in 4 oz of water every 4 hours. Do not exceed 10 tablets in 24 hours or as directed by a doctor. children under 12 years: do not use

Warnings

Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take · more than 4,000 mg of acetaminophen in 24 hours · with other drugs containing acetaminophen · 3 or more alcoholic drinks every day while using this product Allergy alert: Acetaminophen may cause severe skin or severe allergic reactions. Symptoms may include: · skin reddening · blisters · rash · hives · facial swelling · asthma (wheezing) · shock If a skin or general allergic reaction occurs, stop use and seek medical help right away. Sore throat warning : If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly. Do not use to sedate children. Do not use with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist. if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask

Frequently Asked Questions

What is Alka-Seltzer Plus Maximum Strength Sinus Congestion and Pain PowerFast Fizz used for?

Alka-Seltzer Plus Maximum Strength Sinus Congestion and Pain PowerFast Fizz contains chlorpheniramine maleate, dextromethorphan hydrobromide, acetaminophen, phenylephrine hydrochloride. It is a tablet, effervescent taken oral. Consult your doctor for specific uses.

Is Alka-Seltzer Plus Maximum Strength Sinus Congestion and Pain PowerFast Fizz a controlled substance?

Alka-Seltzer Plus Maximum Strength Sinus Congestion and Pain PowerFast Fizz is not classified as a controlled substance by the DEA.

What is the generic name for Alka-Seltzer Plus Maximum Strength Sinus Congestion and Pain PowerFast Fizz?

The generic name for Alka-Seltzer Plus Maximum Strength Sinus Congestion and Pain PowerFast Fizz is chlorpheniramine maleate, dextromethorphan hydrobromide, acetaminophen, phenylephrine hydrochloride. There are no other listed brand versions of chlorpheniramine maleate, dextromethorphan hydrobromide, acetaminophen, phenylephrine hydrochloride.

What is the NDC code for Alka-Seltzer Plus Maximum Strength Sinus Congestion and Pain PowerFast Fizz 325 mg/1?

The NDC (National Drug Code) for Alka-Seltzer Plus Maximum Strength Sinus Congestion and Pain PowerFast Fizz 325 mg/1 is 0280-0055, listed by Bayer HealthCare LLC..

Product NDC

0280-0055

Package NDC

0280-0055-01

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

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