Drugplain

MUCUS RELIEF DM 60 mg/1

dextromethorphan hydrobromide, guaifenesin · TABLET, EXTENDED RELEASE · CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED

No Recall History
Plain English

MUCUS RELIEF DM is a tablet, extended release containing dextromethorphan hydrobromide, guaifenesin at 60 mg/1, taken oral. Manufactured by CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED.

Key Facts

Brand Name
MUCUS RELIEF DM
Generic Name
dextromethorphan hydrobromide, guaifenesin
NDC Code (Product)
51316-671
Manufacturer
CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Strength
60 mg/1
Dosage Form
TABLET, EXTENDED RELEASE
Route
ORAL
Marketing Status
Application #
ANDA207602
Drug Class
Expectorant [EPC]
Marketing Start
12/17/2025

Recall History

No Recall History

Side Effects Reported to FDA

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

dyspnoea579 reports
pneumonia541 reports
nausea498 reports
drug ineffective471 reports
fatigue471 reports
pain443 reports
diarrhoea435 reports
cough383 reports
headache376 reports
off label use373 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

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 crush, chew, or break tablet take with a full glass of water this product can be administered without regards for timing of meals adults and children 12 years of age and older: 1 or 2 tablet every 12 hours; not more than 4 tablets in 24 hours children under 12 years of age: do not use

Warnings

Warnings Do not use for children under 12 years of age 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 accompanied by 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 persistent headache. These could be signs of a serious illness. 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 (1-800-222-1222).

Frequently Asked Questions

What is MUCUS RELIEF DM used for?

MUCUS RELIEF DM contains dextromethorphan hydrobromide, guaifenesin. It is a tablet, extended release taken oral. Consult your doctor for specific uses.

Is MUCUS RELIEF DM a controlled substance?

MUCUS RELIEF DM is not classified as a controlled substance by the DEA.

What is the generic name for MUCUS RELIEF DM?

The generic name for MUCUS RELIEF DM is dextromethorphan hydrobromide, guaifenesin. There are 10 other brand versions of dextromethorphan hydrobromide, guaifenesin.

What is the NDC code for MUCUS RELIEF DM 60 mg/1?

The NDC (National Drug Code) for MUCUS RELIEF DM 60 mg/1 is 51316-671, listed by CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED.

Product NDC

51316-671

Package NDC

51316-671-55

Other MUCUS RELIEF DM Dosages

Other Dextromethorphan Brands

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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)