QCH ADULT TUSSIN DM 542- dextromethorphan hbr, guaifenesin liquid

QCH Adult Tussin DM 542 by

Drug Labeling and Warnings

QCH Adult Tussin DM 542 by is a Otc medication manufactured, distributed, or labeled by Chain Drug Marketing Association Inc., Guardian Drug Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT(S)

Dextromethorphan HBr, USP 20 mg 

Guaifenesin, USP 200 mg 

PURPOSE

Cough suppressant 

Expectorant

USE(S)

• temporarily relieves 
• cough due too minor throat and bronchial irritation as may occur with a cold
• helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes 

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

• cough that occurs with too much phlegm (mucus)
• cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis or emphysema

STOP USE AND ASK DOCTOR IF

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

shake well before using 

do not take more than 6 doses in any 24-hour period 

measure only with dosing cup provided

keep dosing cup with product 

ml=milliliter

this adult product is not intended for use in children under 12 years of age 

• Age: Dose
• adults & children 12 years & over: 20 mL every 4 hours
• children under 12 years: do not use

OTHER INFORMATION

• each 20 mL contains: sodium 15 mg 
• store at 20-25oC (68-77oF)
• do not refrigerate

INACTIVE INGREDIENTS

carboxymethylcellulose sodium, citric acid, FD&C blue 1 dye, FD&C red 40 dye, flavor, glycerin, high fructose corn syrup, menthol, polyethylene glycol, propylene glycol, purified water, sodium benzoate, sodium citrate, sucralose, xanthan gum.

PRINCIPAL DISPLAY PANEL

NDC: 83324-023-04

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

Non- Drowsy

Raspberry  Flavor 

4 FL OZ(118 mL)

NDC: 83324-023-08

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

Non- Drowsy

Raspberry  Flavor 

8 FL OZ(237 mL)

INGREDIENTS AND APPEARANCE

QCH ADULT TUSSIN DM 542 
dextromethorphan hbr, guaifenesin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83324-023
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	20 mg  in 20 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	200 mg  in 20 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C RED NO. 40 (UNII: WZB9127XOA)
GLYCERIN (UNII: PDC6A3C0OX)
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)
MENTHOL (UNII: L7T10EIP3A)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
SUCRALOSE (UNII: 96K6UQ3ZD4)
XANTHAN GUM (UNII: TTV12P4NEE)

Product Characteristics
Color	RED	Score
Shape		Size
Flavor	RASPBERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83324-023-04	1 in 1 CARTON	05/08/2024
1		118 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 83324-023-08	1 in 1 CARTON	05/08/2024
2		237 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	part341	05/08/2024

Labeler - Chain Drug Marketing Association Inc. (011920774)

Establishment
Name	Address	ID/FEI	Business Operations
Guardian Drug Company		119210276	MANUFACTURE(83324-023)