CHILDRENS MUCUS AND COUGH RELIEF- guaifenesin and dextromethorphan hydrobromide liquid 
Chain Drug Manufacturing Assn

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Quality Choice Children's Mucus &

Cough Relief Cherry Flavor 4 FL OZ
(118 mL)

Drug Facts

Active ingredients (in each 5 mL)

Purposes

Dextromethorphan HBr 5 mg

Cough suppressant

Guaifenesin 100 mg

Expectorant

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 your child get to sleep

Warnings

Do not use in a child who is 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 child's prescription drug contains an MAOI, ask a doctor or pharmacist before giving this product.

Ask a doctor before use if the child has

cough that occurs with too much phlegm (mucus)
persistent or chronic cough such as occurs with asthma

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.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

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
mL = milliliter
AgeDose

children 6 years to under 12 years

5 mL – 10 mL every 4 hours

children 4 years to under 6 years

2.5 mL – 5 mL every 4 hours

children under 4 years

do not use

Other information

each 5 mL contains: sodium 3 mg
Tamper -evident: do not use if printed inner seal under cap is torn or missing
store at room temperature
do not refrigerate
dosing cup provided

Inactive ingredients

Anhydrous citric acid, edetate disodium, FD&C Red#40, flavors, potassium citrate, propylene glycol, purified water, sodium benzoate, sorbitol, sucralose, xanthan gum

PRINCIPAL DISPLAY PANEL - 118 mL Bottle Carton

NDC 63868-771-04

Compare to the Active ingredient in Children’s Mucinex Cough*

Children's

Mucus &Cough Relief

Cough Suppressant

Expectorant

Dextromethorphan HBr

Guaifenesin

Each Dose of Cherry Flavored

Children's

Mucus & Cough Relief:

Controls Cough
Relieves Chest Congestion
Breaks up Mucus


Alcohol-free

See New Dosing information

Cherry
Flavor

4 FL OZ
(118 mL)

IMPORTANT: Keep this carton for future reference on full labeling.

DOSAGE CUP INCLUDED

Distributed by C.D.M.A., Inc©

43157 W. Nine Mile

Novi, MI 48376-0995

www.qualitychoice.com

Questions: 248-449-9300

*This product is not manufactured or distributed by Reckitt Benckiser, distributor of Children’s Mucinex.®

QC 100% Satisfaction Guaranteed.

Quality Choice Children's Mucus and Cough Relief Cherry Flavor 4 FL OZ
CHILDRENS MUCUS AND COUGH RELIEF 
guaifenesin and dextromethorphan hydrobromide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-771
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE5 mg  in 5 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN100 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
POTASSIUM CITRATE (UNII: EE90ONI6FF)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SORBITOL (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Product Characteristics
ColorREDScore    
ShapeSize
FlavorCHERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63868-771-041 in 1 CARTON10/19/2015
1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01210/19/2015
Labeler - Chain Drug Manufacturing Assn (011920774)

Revised: 11/2023
Document Id: 5807d840-01ce-4c52-9884-3286958530ce
Set id: 06822a28-3f82-471d-8db5-c5981b263a03
Version: 6
Effective Time: 20231109
 
Chain Drug Manufacturing Assn