Drugplain

KROGER Mucus Relief DM Maximum Strength 20 mg/20mL

Dextromethorphan HBr and Guaifenesin · SOLUTION · KROGER COMPANY

No Recall History
Plain English

KROGER Mucus Relief DM Maximum Strength is a solution containing dextromethorphan hbr and guaifenesin at 20 mg/20mL, taken oral. Manufactured by KROGER COMPANY.

Key Facts

Brand Name
KROGER Mucus Relief DM Maximum Strength
Generic Name
Dextromethorphan HBr and Guaifenesin
NDC Code (Product)
41226-739
Manufacturer
KROGER COMPANY
Strength
20 mg/20mL
Dosage Form
SOLUTION
Route
ORAL
Marketing Status
Application #
M012
Drug Class
Expectorant [EPC]
Marketing Start
04/05/2024

Recall History

No Recall History

Side Effects Reported to FDA

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

cardiac arrest5 reports
respiratory arrest5 reports
intentional drug misuse2 reports
arrhythmia supraventricular1 reports
completed suicide1 reports
device information output issue1 reports
device use confusion1 reports
drug abuse1 reports
product commingling1 reports
product label confusion1 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 take more than 6 doses in any 24-hour period measure only with dosing cup provided do not use dosing cup with other products dose as follows or as directed by a doctor mL = milliliter adults and children 12 years and older: 20 mL every 4 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 persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis or emphysema cough that occurs with 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 that lasts. These could be signs of a serious condition. 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 at 1-800-222-2222.

Frequently Asked Questions

What is KROGER Mucus Relief DM Maximum Strength used for?

KROGER Mucus Relief DM Maximum Strength contains Dextromethorphan HBr and Guaifenesin. It is a solution taken oral. Consult your doctor for specific uses.

Is KROGER Mucus Relief DM Maximum Strength a controlled substance?

KROGER Mucus Relief DM Maximum Strength is not classified as a controlled substance by the DEA.

What is the generic name for KROGER Mucus Relief DM Maximum Strength?

The generic name for KROGER Mucus Relief DM Maximum Strength is Dextromethorphan HBr and Guaifenesin. There are 11 other brand versions of Dextromethorphan HBr and Guaifenesin.

What is the NDC code for KROGER Mucus Relief DM Maximum Strength 20 mg/20mL?

The NDC (National Drug Code) for KROGER Mucus Relief DM Maximum Strength 20 mg/20mL is 41226-739, listed by KROGER COMPANY.