Drugplain

Mucinex Fast-Max Severe Congestion and Cough 20 mg/20mL

dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride · SOLUTION · Reckitt Benckiser LLC

No Recall History
Plain English

Mucinex Fast-Max Severe Congestion and Cough is an over-the-counter liquid medication that combines an expectorant to help thin mucus, a cough suppressant, and a nasal decongestant to relieve congestion and cough symptoms. It is taken by mouth and is commonly used to provide temporary relief from symptoms associated with colds and upper respiratory congestion.

Key Facts

Brand Name
Mucinex Fast-Max Severe Congestion and Cough
Generic Name
dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
NDC Code (Product)
63824-540
Manufacturer
Reckitt Benckiser LLC
Strength
20 mg/20mL
Dosage Form
SOLUTION
Route
ORAL
Marketing Status
Application #
M012
Drug Class
Expectorant [EPC]
Marketing Start
11/01/2017

Recall History

No Recall History

Side Effects Reported to FDA

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

dizziness15 reports
dyspnoea10 reports
drug ineffective9 reports
insomnia7 reports
nausea6 reports
diarrhoea5 reports
heart rate increased5 reports
blood glucose increased4 reports
blood pressure increased4 reports
epistaxis4 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses Uses: ■ helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive Temporarily relieves: ■ cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants ■ the intensity of coughing ■ the impulse to cough to help you get to sleep

Dosage & Administration

Directions ■ do not take more than 12 capsules in any 24-hour period ■ adults and children 12 years of age and over: take 2 capsules every 4 hours ■ children under 12 years of age: do not use

Warnings

Do not use: ■ 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 a doctor or pharmacist before taking this product. Ask a doctor before use if you have ■ persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema ■ cough that occurs with too much phlegm (mucus) When using this product do not use more than directed Stop use and ask a doctor if ■ cough lasts more than 7 days, comes back, or occurs with fever, rash, or headache that lasts. These could be signs of a serious condition. If pregnant or breast-feeding , ask a health professional before use. Keep out of reach of children . In case of overdose, get medical help or contact a Poison Control Center right away.

Frequently Asked Questions

What is Mucinex Fast-Max Severe Congestion and Cough used for?

Mucinex Fast-Max Severe Congestion and Cough is an over-the-counter liquid medication that combines an expectorant to help thin mucus, a cough suppressant, and a nasal decongestant to relieve congestion and cough symptoms. It is taken by mouth and is commonly used to provide temporary relief from symptoms associated with colds and upper respiratory congestion.

Is Mucinex Fast-Max Severe Congestion and Cough a controlled substance?

Mucinex Fast-Max Severe Congestion and Cough is not classified as a controlled substance by the DEA.

What is the generic name for Mucinex Fast-Max Severe Congestion and Cough?

The generic name for Mucinex Fast-Max Severe Congestion and Cough is dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride. There are 12 other brand versions of dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride.

What is the NDC code for Mucinex Fast-Max Severe Congestion and Cough 20 mg/20mL?

The NDC (National Drug Code) for Mucinex Fast-Max Severe Congestion and Cough 20 mg/20mL is 63824-540, listed by Reckitt Benckiser LLC.

Product NDC

63824-540

Package NDC

63824-540-66

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

Data from openFDA · Public domain (CC0 1.0)