Mucus Relief Extended Release Maximum Strength 1200 mg/1
Guaifenesin · TABLET · CARDINAL HEALTH 110, LLC. DBA LEADER 70000
Mucus Relief Extended Release Maximum Strength is a tablet containing guaifenesin at 1200 mg/1, taken oral. Manufactured by CARDINAL HEALTH 110, LLC. DBA LEADER 70000.
Key Facts
- Brand Name
- Mucus Relief Extended Release Maximum Strength
- Generic Name
- Guaifenesin
- NDC Code (Product)
70000-0479- Manufacturer
- CARDINAL HEALTH 110, LLC. DBA LEADER 70000
- Strength
- 1200 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- ANDA207342
- Drug Class
- Expectorant [EPC]
- Marketing Start
- 01/31/2019
Recall History
No Recall HistorySide 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 makes coughs more productive.
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 the timing of meals adults and children 12 years of age and over: 1 tablet every 12 hours. Do not exceed 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. 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) 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 Extended Release Maximum Strength used for?
Mucus Relief Extended Release Maximum Strength contains Guaifenesin. It is a tablet taken oral. Consult your doctor for specific uses.
Is Mucus Relief Extended Release Maximum Strength a controlled substance?
Mucus Relief Extended Release Maximum Strength is not classified as a controlled substance by the DEA.
What is the generic name for Mucus Relief Extended Release Maximum Strength?
The generic name for Mucus Relief Extended Release Maximum Strength is Guaifenesin. There are 12 other brand versions of Guaifenesin.
What is the NDC code for Mucus Relief Extended Release Maximum Strength 1200 mg/1?
The NDC (National Drug Code) for Mucus Relief Extended Release Maximum Strength 1200 mg/1 is 70000-0479, listed by CARDINAL HEALTH 110, LLC. DBA LEADER 70000.
Other Guaifenesin Brands
See all →- Guaifenesin and Dextromethorphan Hydrobromide10 mg/5mL72162-2277
- basic care mucus er600 mg/172288-298
- basic care mucus er max1200 mg/172288-613
- Pharbinex-DM20 mg/173057-381
- Mucus Relief DM Extended Release Caplets30 mg/10536-1161
- MUCUS RELIEF - DM MAXIMUM STRENGTH60 mg/173581-405
- BACZOL EXPECTORANT200 mg/5mL76864-209
- Guaifenesin and Pseudoephedrine HCl600 mg/179481-1002
- Meijer Adult Mucus Plus chest congestion200 mg/10mL79481-7430
- Tussin Mucus and Chest Congestion Sugar Free200 mg/10mL82568-0012
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)