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Sun Mark Tussin DMcough and chest congestion

Dosage form
SOLUTION
Labeler
Central Texas Community Health Centers
Label updated
2017-11-17
Retrieved
2026-09-07
Active ingredients
DEXTROMETHORPHAN HYDROBROMIDE · GUAIFENESIN
View original label and images on DailyMed ↗
Active ingredients (in each 10 mL)

Dextromethorphan HBr, USP 20 mg

Guaifenesin, USP 200 mg

Purposes

Cough suppressant

Expectorant

Uses
  • •temporarily relieves cough due to 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 you have

  • •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 a doctor if

cough lasts for more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. A persistent cough may be a sign 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 (1-800-222-1222).

Directions
  • •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 and children

12 years and over

10 mL every 4 hours

children under 12 years

do not use

Other information
  • •each 10 mL contains: sodium 6 mg
  • •store at 20-25°C (68-77°F).
  •  Do not refrigerate.
Inactive ingredients

anhydrous citric acid, FD&C red no. 40, flavor, glycerin, high fructose corn syrup, menthol, propylene glycol, purified water, sodium benzoate, sodium citrate, sucralose

Questions or comments?

1-800-719-9260

PRINCIPAL DISPLAY PANEL - 118 ml Bottle Carton Label

CommUnityCare Federally Qualified Health Centers

TUSSIN
DM 118ml

Date:

Name:

Dr.

TAKE AS DIRECTED.

123456

1/1/01

TUSSIN DM 118ml NDC 76413-329-01

Batch: 123456
Lot: 123456
Exp: 1/1/01
SUNMARK

Federal law prohibits the transfer of this drug to any other person than the patient for whom prescribed.

[Image in the official label — see DailyMed source]

DailyMed Set ID: 3521aaab-a291-41db-9ee3-107e163e9a88 · Version 1
NDC: 76413-329