Drugplain

Mucus Relief D 600 mg/1

Guaifenesin and Pseudoephedrine HCL · TABLET, EXTENDED RELEASE · Walgreens Company

1 Recall on Record
Plain English

Mucus Relief D is a tablet, extended release containing guaifenesin and pseudoephedrine hcl at 600 mg/1, taken oral. Manufactured by Walgreens Company.

Key Facts

Brand Name
Mucus Relief D
Generic Name
Guaifenesin and Pseudoephedrine HCL
NDC Code (Product)
0363-1604
Manufacturer
Walgreens Company
Strength
600 mg/1
Dosage Form
TABLET, EXTENDED RELEASE
Route
ORAL
Marketing Status
Application #
ANDA208369
Drug Class
Expectorant [EPC]
Marketing Start
08/13/2019

Recall History

1 Recall on Record
Class III01/10/2022

Dr. Reddy's Laboratories, Inc.

Subpotent drug

TerminatedVoluntary: Firm initiated

Side Effects Reported to FDA

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

pain5 reports
anxiety4 reports
deep vein thrombosis4 reports
myocardial infarction4 reports
pulmonary embolism4 reports
cholecystitis chronic3 reports
death3 reports
depression3 reports
injury3 reports
pneumonia3 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 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 Relief D used for?

Mucus Relief D contains Guaifenesin and Pseudoephedrine HCL. It is a tablet, extended release taken oral. Consult your doctor for specific uses.

Is Mucus Relief D a controlled substance?

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

What is the generic name for Mucus Relief D?

The generic name for Mucus Relief D is Guaifenesin and Pseudoephedrine HCL. There are 10 other brand versions of Guaifenesin and Pseudoephedrine HCL.

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

The NDC (National Drug Code) for Mucus Relief D 600 mg/1 is 0363-1604, listed by Walgreens Company.

Product NDC

0363-1604

Package NDC

0363-1604-15

Other Guaifenesin 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)