QCH MAXIMUM STRENGTH MUCUS RELIEF DM 628 - dextromethorphan hbr, guaifenesin liquid 
Chain Drug Marketing Association Inc.

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QCH Maximum Strength Mucus Relief DM 628

ACTIVE INGREDIENTS (in each 20 mL)

Dextromethorphan HBr, 20 mg

Guaifenesin, 400 mg


PURPOSE

Cough Suppressant

Expectorant


USE(S)


WARNINGS

.

DO NOT USE

ASK A DOCTOR BEFORE USE IF

WHEN USING THIS PRODUCT

STOP USE AND ASK DOCTOR IF

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.

DIRECTIONS







OTHER INFORMATION

INACTIVE INGREDIENTS

citric acid anhydrous, dextrose, D&C red # 33, FD&C Red #40,  flavors, glycerin, methylparaben, potassium sorbate, propylene glycol, propylparaben, purified water, saccharin sodium, sodium hydroxide, sorbitol, sucralose, xanthan gum.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 83324-026-06

QUALITY CHOICE®

*Compare to the Active Ingredient Maximum  Strength Mucinex Fast Max DM®  

 

Maximum Strength
Mucus
Relief


Cough Suppressant / Expectorant

Dextromethorphan HBr, 20 mg Per 20 mL
Guaifenesin, 400 mg Per 20 mL

Helps Control Cough 

Relieves Chest Congestion 

Thins and Loosens Mucus

Cherry Flavor

6 FL OZ (177 mL)

628-front-qch


628-back-qch



 


QCH MAXIMUM STRENGTH MUCUS RELIEF DM 628 
dextromethorphan hbr, guaifenesin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83324-026
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE20 mg  in 20 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN400 mg  in 20 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
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:83324-026-06177 mL in 1 BOTTLE; Type 0: Not a Combination Product04/26/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH DRUGpart34104/26/2024
Labeler - Chain Drug Marketing Association Inc. (011920774)
Establishment
NameAddressID/FEIBusiness Operations
Guardian Drug Company119210276MANUFACTURE(83324-026)

Revised: 4/2024
Document Id: a2795bf5-34c6-4de6-b9e5-53a23d18e357
Set id: a2795bf5-34c6-4de6-b9e5-53a23d18e357
Version: 1
Effective Time: 20240426
 
Chain Drug Marketing Association Inc.