QCH ADULT TUSSIN DM SUGAR FREE 545 - dextromethorphan hbr, guaifenesin liquid 
Chain Drug Marketing Association Inc.

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QCH Adult Tussin DM Sugar Free 545

ACTIVE INGREDIENT(S)

Dextromethorphan HBr, USP 20 mg 

Guaifenesin, USP 200 mg

PURPOSE

Cough suppressant

Expectorant

USE(S)


WARNINGS

.

DO NOT USE

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

STOP USE AND ASK DOCTOR IF

cough  lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache.

These could be signs of a serious condition.




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


Age Dose 
 adults & children  12 years & over 20 mL every 4 Hours
 Children under 12 years do not use

OTHER INFORMATION

INACTIVE INGRADIENTS

carboxymethylcellulose sodium, citric acid, flavor, glycerin, menthol, polyethylene glycol, propylene glycol, purified water , sodium benzoate, sodium citrate, sorbitol, sucralose, xanthan gum.

PRINCIPAL DISPLAY PANEL

NDC 83324-025-04

QUALITY CHOICE

* Compare to the Active Ingredients in Robitussin® DM

Adult Tussin DM

Cough Suppressant/ Expectorant

Dextromethorphan HBr 20 mg per 20 mL 

Guaifenesin 200 mg per 20 mL

For Ages 12 & Over 

Helps Control Cough 

Relieves Chest Congestion 

Thins  and Loosens Mucus

Specially Formulated for Diabetics

Non-Drowsy

Sugar Free Dye Free

Peppermint Flavor

4 FL OZ (118 mL)

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545-qch-carton.jpg

QCH ADULT TUSSIN DM SUGAR FREE 545 
dextromethorphan hbr, guaifenesin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83324-025
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) GUAIFENESIN200 mg  in 20 mL
Inactive Ingredients
Ingredient NameStrength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
GLYCERIN (UNII: PDC6A3C0OX)  
MENTHOL (UNII: L7T10EIP3A)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
SORBITOL (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Product Characteristics
Color    Score    
ShapeSize
FlavorPEPPERMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83324-025-041 in 1 CARTON05/08/2024
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 Drugpart34105/08/2024
Labeler - Chain Drug Marketing Association Inc. (011920774)
Establishment
NameAddressID/FEIBusiness Operations
Guardian Drug Company119210276MANUFACTURE(83324-025)

Revised: 5/2024
Document Id: 86cc0533-cf2e-4227-8123-179cb12272a2
Set id: 17cb91f0-32ec-9e0f-e063-6394a90a0509
Version: 2
Effective Time: 20240508
 
Chain Drug Marketing Association Inc.