Active Ingredients (In Each 20 Ml)
Dextromethorphan HBr 20 mg
Guaifenesin 400 mg
Phenylephrine HCI 10 mg
Qch Maximum Strength Mucus Relief 617 Liquid
FDA Label NDC 83324-144
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Chain Drug Marketing Association Inc. for the product Qch Maximum Strength Mucus Relief 617 (NDC 83324-144). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients (in each 20 ml), purpose, use(s), warnings, do not use, ask a doctor before use if you have, when using this product, stop use and ask doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Cough suppressant
Expectorant
Nasal decongestant
Use(S)
• helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes 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
• nasal congestion due to a cold
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
• 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 that occurs with too much phlegm (mucus)
When Using This Product
• do not use more than directed
Stop Use And Ask Doctor If
- nervousness, dizziness or sleeplessness occur
- symptoms do not get better within 7 days or occur with fever
- cough comes back, or occurs with rash or persistent headache. These could be signs of a serious condition.
Pregnancy/Breastfeeding
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.
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
• Adults and children 12 years and older: 20 ml in dosing cup provided every 4 hours .
• Children under 12 years of age: Do not use
Other Information
• each 20 ml contains: sodium 20 mg
• store between 15-30°C (59-86°F)
• do not refrigerate
• dosing cup provided
Inactive Ingredients
citric acid anhydrous, edetate disodium, FD&C blue #1, FD&C red #40, flavors, glycerin, propylene glycol, propyl gallate, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose, xanthan gum.
Principal Display Panel
NDC 83324-144-06
QC® QUALITY CHOICE
*Compare to the Active Ingredients in Maximum Strength Mucinex® Fax MaxTM Severe Congestion & Cough
Maximum Strength Mucus Relief Sever Congestion & Cough
Dextromethorphan HBr 20 mg - Cough suppressant
Guaifenesin 400 mg - Expectorant
Phenylephrine HCI 10 mg - Nasal decongestant
Helps Control Cough
Relieves Nasal & Chest Congestion
Thins & Loosens Mucus
6 FL OZ (177 mL)
617-qch-fl.jpg (617 Qch Fl)
617-qch-bl.jpg (617 Qch Bl)
* Please review the disclaimer below.
