CHILDRENS MUCUS RELIEF  CHEST CONGESTION- guaifenesin solution 
Chain Drug Manufacturing Assn

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QC Quality Choice Children’s
Mucus Relief Expectorant Grape Flavor 4 FL OZ (118mL)

Drug Facts

Active ingredient (in each 5 mL)

Guaifenesin, USP 100 mg

Purpose

Expectorant

Uses

helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive

Warnings

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 ifcough 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.

Directions

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

Inactive ingredients

anhydrous citric acid, edetate disodium, FD&C Blue #1, FD&C Red #40, flavors, potassium citrate propylene glycol, purified water, sodium benzoate ,sorbitol, sucralose, xanthan gum.

PRINCIPAL DISPLAY PANEL - 118 mL Bottle Carton

QC QUALITY CHOICE NDC 63868-770-04

Children's
Mucus relief

Expectorant

Guaifenesin

Oral Solution, USP

Each Dose of Grape Flavored

Children’s Mucus Relief:

Relieves Chest Congestion


Alcohol Free

Grape
Flavor

4 FL OZ
(118 mL)

IMPORTANT:

Keep this carton for future reference on full labeling.

DOSAGE CUP INCLUDED

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

Distributed by C.D.M.A.,Inc©

43157 W. Nine Mile

Novi, MI 48376-0995

www.qualitychoice.com

Questions: 248-449-9300

QC 100% Satisfaction Guaranteed.

Quality Choice Childrens Mucus Relief Expectorant Grape Flavor 4 FL OZ
CHILDRENS MUCUS RELIEF   CHEST CONGESTION
guaifenesin solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-770
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
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 BLUE NO. 1 (UNII: H3R47K3TBD)  
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
ColorpurpleScore    
ShapeSize
FlavorGRAPEImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63868-770-041 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: 12/2025
Document Id: 451da3de-0781-522d-e063-6394a90a3537
Set id: 034d39c0-9aad-4dff-a158-a041b9f0504f
Version: 8
Effective Time: 20251204
 
Chain Drug Manufacturing Assn