Drugplain

Mucinex Nightshift Sinus Maximum Strength 325 mg/1

Acetaminophen, Dextromethorphan Hydrobromide, and Triprolidine Hydrochloride · TABLET, COATED · RB Health (US) LLC

No Recall HistoryCurrently in Shortage
Plain English

Mucinex Nightshift Sinus Maximum Strength is a tablet, coated containing acetaminophen, dextromethorphan hydrobromide, and triprolidine hydrochloride at 325 mg/1, taken oral. Manufactured by RB Health (US) LLC.

Key Facts

Brand Name
Mucinex Nightshift Sinus Maximum Strength
Generic Name
Acetaminophen, Dextromethorphan Hydrobromide, and Triprolidine Hydrochloride
NDC Code (Product)
72854-209
Manufacturer
RB Health (US) LLC
Strength
325 mg/1
Dosage Form
TABLET, COATED
Route
ORAL
Marketing Status
Application #
M012
Marketing Start
05/01/2025

Recall History

No Recall History

Side Effects Reported to FDA

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

anaphylactic reaction1 reports
chest discomfort1 reports
dyspnoea1 reports
erythema1 reports
fatigue1 reports
therapeutic response unexpected1 reports
vomiting1 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses temporarily relieves these common cold and flu symptoms: cough nasal congestion minor aches and pains sore throat headache sinus congestion and pressure runny nose sneezing itching of the nose or throat itchy, watery eyes due to hay fever temporarily reduces fever controls cough to help you get to sleep

Dosage & Administration

Directions do not take more than directed (see Overdose warning ) do not take more than 8 caplets in any 24-hour period adults and children 12 years of age and over: take 2 caplets every 4 hours children under 12 years of age: do not use

Warnings

Warnings Liver warning This product contains acetaminophen. Severe liver damage may occur if you take: more than 4,000 mg 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 (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 a doctor or pharmacist before taking this product. Ask a doctor before use if you have liver disease heart disease

Frequently Asked Questions

What is Mucinex Nightshift Sinus Maximum Strength used for?

Mucinex Nightshift Sinus Maximum Strength contains Acetaminophen, Dextromethorphan Hydrobromide, and Triprolidine Hydrochloride. It is a tablet, coated taken oral. Consult your doctor for specific uses.

Is Mucinex Nightshift Sinus Maximum Strength a controlled substance?

Mucinex Nightshift Sinus Maximum Strength is not classified as a controlled substance by the DEA.

What is the generic name for Mucinex Nightshift Sinus Maximum Strength?

The generic name for Mucinex Nightshift Sinus Maximum Strength is Acetaminophen, Dextromethorphan Hydrobromide, and Triprolidine Hydrochloride. There are 5 other brand versions of Acetaminophen, Dextromethorphan Hydrobromide, and Triprolidine Hydrochloride.

What is the NDC code for Mucinex Nightshift Sinus Maximum Strength 325 mg/1?

The NDC (National Drug Code) for Mucinex Nightshift Sinus Maximum Strength 325 mg/1 is 72854-209, listed by RB Health (US) LLC.