QCH Maximum Strength Mucus Relief 617
Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl · Liquid · Oral
Active ingredient
(in each 20 mL) Dextromethorphan HBr 20 mg Guaifenesin 400 mg Phenylephrine HCI 10 mg
Purpose
Cough suppressant Expectorant Nasal decongestant
Uses
• 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
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
• 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 a doctor
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 or breast-feeding
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 olde r: 20 ml in dosing cup provided every 4 hours .
• Children under 12 years of age : Do not use
Inactive ingredients
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.
Label text from the FDA structured product label by Chain Drug Marketing Association Inc. (revised Sep 6, 2024). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Dextromethorphan Hydrobromide in 1 product
- Guaifenesin in 1 product
- Phenylephrine Hydrochloride in 1 product
QCH Maximum Strength Mucus Relief 617 NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 83324-144 | Dextromethorphan Hydrobromide 20 mg/20mL; Guaifenesin 400 mg/20mL; Phenylephrine Hydrochloride 10 mg/20mL Liquid | Chain Drug Marketing Association Inc. | OTC MONOGRAPH DRUG |
Frequently asked questions
What is QCH Maximum Strength Mucus Relief 617 used for?
• 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
Who makes QCH Maximum Strength Mucus Relief 617?
QCH Maximum Strength Mucus Relief 617 is listed by 1 labeler in the FDA NDC directory, including Chain Drug Marketing Association Inc..