Drugplain

Mucinex Rapid Clear Daytime Pain, Headache, and Cough 325 mg/1

Acetaminophen, Dextromethorphan Hydrobromide · CAPSULE, LIQUID FILLED · Reckitt Benckiser LLC

No Recall HistoryCurrently in Shortage
Plain English

Mucinex Rapid Clear Daytime Pain, Headache, and Cough is a prescription capsule, liquid filled containing acetaminophen, dextromethorphan hydrobromide at 325 mg/1, taken oral. Manufactured by Reckitt Benckiser LLC.

Key Facts

Brand Name
Mucinex Rapid Clear Daytime Pain, Headache, and Cough
Generic Name
Acetaminophen, Dextromethorphan Hydrobromide
NDC Code (Product)
72854-214
Manufacturer
Reckitt Benckiser LLC
Strength
325 mg/1
Dosage Form
CAPSULE, LIQUID FILLED
Route
ORAL
Marketing Status
HUMAN OTC DRUG
Application #
M012
Drug Class
Sigma-1 Agonist [EPC]; Sigma-1 Receptor Agonists [MoA]
Marketing Start
06/01/2025

Recall History

No Recall History

Side Effects Reported to FDA

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

asthenopia1 reports
epistaxis1 reports
feeling abnormal1 reports
incorrect dose administered1 reports
poor quality product administered1 reports
product complaint1 reports
somnolence1 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses temporarily relieves these common cold and flu symptoms: ■ 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 ■ minor aches and pains ■ sore throat ■ headache ■ temporarily reduces fever

Dosage & Administration

Directions do not take more than directed (see Overdose warning ) do not take more than 12 liquid gels in any 24-hour period adults and children 12 years of age and over: take 2 liquid gels every 4 hours children under 12 years of age: do not use

Warnings

Warnings This product contains acetaminophen. Severe liver damage may occur if you take: more than 12 liquid gels in 24 hours, which is the maximum daily amount with other drugs containing acetaminophen 3 or more alcoholic drinks daily while using this product Liver warning This product contains acetaminophen. Severe liver damage may occur if you take: more than 12 liquid gels in 24 hours, which is the maximum daily amount with other drugs containing acetaminophen 3 or more alcoholic drinks daily while using this product Allergy alert Acetaminophen may cause severe skin reactions. Symptoms may include: skin reddening blisters rash If a skin 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 with any other drug containing acetaminophen (precription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist. if you are now taking a precription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditio

Frequently Asked Questions

What is Mucinex Rapid Clear Daytime Pain, Headache, and Cough used for?

Mucinex Rapid Clear Daytime Pain, Headache, and Cough contains Acetaminophen, Dextromethorphan Hydrobromide. It is a capsule, liquid filled taken oral. Consult your doctor for specific uses.

Is Mucinex Rapid Clear Daytime Pain, Headache, and Cough a controlled substance?

Mucinex Rapid Clear Daytime Pain, Headache, and Cough is not classified as a controlled substance by the DEA.

What is the generic name for Mucinex Rapid Clear Daytime Pain, Headache, and Cough?

The generic name for Mucinex Rapid Clear Daytime Pain, Headache, and Cough is Acetaminophen, Dextromethorphan Hydrobromide. There are 12 other brand versions of Acetaminophen, Dextromethorphan Hydrobromide.

What is the NDC code for Mucinex Rapid Clear Daytime Pain, Headache, and Cough 325 mg/1?

The NDC (National Drug Code) for Mucinex Rapid Clear Daytime Pain, Headache, and Cough 325 mg/1 is 72854-214, listed by Reckitt Benckiser LLC.