Mucinex DM 30 mg/1
DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN · TABLET, EXTENDED RELEASE · Navajo Manufacturing Company Inc.
Mucinex DM is a tablet, extended release containing dextromethorphan hydrobromide, guaifenesin at 30 mg/1, taken oral. Manufactured by Navajo Manufacturing Company Inc..
Key Facts
- Brand Name
- Mucinex DM
- Generic Name
- DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN
- NDC Code (Product)
67751-171- Manufacturer
- Navajo Manufacturing Company Inc.
- Strength
- 30 mg/1
- Dosage Form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- NDA021620
- Drug Class
- Expectorant [EPC]
- Marketing Start
- 09/23/2016
Recall History
Reckitt Benckiser LLC
Defective container: A customer complaint revealed the presence of a defective seal on the top of a Mucinex pouch
Family Dollar Stores, Llc.
CGMP Deviations: product held outside appropriate storage temperature conditions.
Side Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Full Prescribing Information
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 tablet every 12 hours; not more than 2 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.
Frequently Asked Questions
What is Mucinex DM used for?
Mucinex DM contains DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN. It is a tablet, extended release taken oral. Consult your doctor for specific uses.
Is Mucinex DM a controlled substance?
Mucinex DM is not classified as a controlled substance by the DEA.
What is the generic name for Mucinex DM?
The generic name for Mucinex DM is DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN. There are 12 other brand versions of DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN.
What is the NDC code for Mucinex DM 30 mg/1?
The NDC (National Drug Code) for Mucinex DM 30 mg/1 is 67751-171, listed by Navajo Manufacturing Company Inc..
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)