Drugplain

MUCUS D 600 mg/1

guaifenesin and pseudoephedrine hydrochloride · TABLET, MULTILAYER, EXTENDED RELEASE · CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED

No Recall History
Plain English

MUCUS D is a tablet, multilayer, extended release containing guaifenesin and pseudoephedrine hydrochloride at 600 mg/1, taken oral. Manufactured by CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED.

Key Facts

Brand Name
MUCUS D
Generic Name
guaifenesin and pseudoephedrine hydrochloride
NDC Code (Product)
51316-878
Manufacturer
CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Strength
600 mg/1
Dosage Form
TABLET, MULTILAYER, EXTENDED RELEASE
Route
ORAL
Marketing Status
Application #
ANDA214407
Drug Class
Expectorant [EPC]
Marketing Start
04/04/2025

Recall History

No Recall History

Side Effects Reported to FDA

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

drug ineffective21 reports
insomnia18 reports
underdose14 reports
nausea9 reports
dizziness7 reports
off label use7 reports
pruritus7 reports
rash7 reports
headache6 reports
anxiety5 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 nasal congestion due to: • common cold • hay fever • upper respiratory allergies • temporarily restores freer breathing through the nose • promotes nasal and/or sinus drainage • temporarily relieves sinus congestion and pressure

Dosage & Administration

Directions • do not crush, chew, or break tablet • take with a full glass of water • this product can be administered without regard for timing of meals • adults and children 12 years and older: 2 tablets 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 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 • heart disease • high blood pressure • thyroid disease • diabetes • trouble urinating due to an enlarged prostate gland • 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 • you get nervous, dizzy, or sleepless • symptoms do not get better within 7 days, come back or occur with a 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 D used for?

MUCUS D contains guaifenesin and pseudoephedrine hydrochloride. It is a tablet, multilayer, extended release taken oral. Consult your doctor for specific uses.

Is MUCUS D a controlled substance?

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

What is the generic name for MUCUS D?

The generic name for MUCUS D is guaifenesin and pseudoephedrine hydrochloride. There are 11 other brand versions of guaifenesin and pseudoephedrine hydrochloride.

What is the NDC code for MUCUS D 600 mg/1?

The NDC (National Drug Code) for MUCUS D 600 mg/1 is 51316-878, listed by CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED.