Leader Mucus Relief DM 30 mg/1

dextromethorphan hydrobromide, guaifenesin · TABLET, EXTENDED RELEASE · Cardinal Health 110, LLC. dba Leader

No Recall History

Plain English

Leader Mucus Relief DM is a tablet, extended release containing dextromethorphan hydrobromide, guaifenesin at 30 mg/1, taken oral. Manufactured by Cardinal Health 110, LLC. dba Leader.

Key Facts

Brand Name: Leader Mucus Relief DM
Generic Name: dextromethorphan hydrobromide, guaifenesin
NDC Code (Product): 70000-0722
Manufacturer: Cardinal Health 110, LLC. dba Leader
Strength: 30 mg/1
Dosage Form: TABLET, EXTENDED RELEASE
Route: ORAL
Marketing Status
Application #: ANDA207602
Drug Class: Expectorant [EPC]
Marketing Start: 03/08/2025

Recall History

No Recall History

Side Effects Reported to FDA

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

blister1 reports

clonus1 reports

dermatitis1 reports

diarrhoea1 reports

drug abuse1 reports

erythema1 reports

fixed eruption1 reports

hepatic function abnormal1 reports

hyperchloraemia1 reports

hypersensitivity1 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 regard for timing of meals • adults and children 12 years and older: 1 or 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 • 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 Leader Mucus Relief DM used for?

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

Is Leader Mucus Relief DM a controlled substance?

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

What is the generic name for Leader Mucus Relief DM?

The generic name for Leader Mucus Relief DM is dextromethorphan hydrobromide, guaifenesin. There are 12 other brand versions of dextromethorphan hydrobromide, guaifenesin.

What is the NDC code for Leader Mucus Relief DM 30 mg/1?

The NDC (National Drug Code) for Leader Mucus Relief DM 30 mg/1 is 70000-0722, listed by Cardinal Health 110, LLC. dba Leader.

Product NDC

70000-0722

Package NDC

70000-0722-1

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)