Tussin dm cough and chest congestion capsule, liquid filled

Spl unclassified section

Drug Facts

Active ingredients (in each softgel)

Dextromethorphan HBr, USP 10 mg

Guaifenesin, USP 200 mg


Cough suppressant



  • 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


Otc - do not use section

Do not use ifyou 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

Otc - stop use section

Stop use and ask a doctor ifcough lasts for more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.

Otc - pregnancy or breast feeding section

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.


  • do not take more than 12 softgels in any 24-hour period
  • this adult product is not intended for use in children under 12 years of age



adults and children 12 years and over

2 softgels every 4 hours

children under 12 years

do not use

Other information

  • store at room temperature 15-30C (59-86F)
  • avoid excessive heat above 40C (104F)

Inactive ingredients

FD&C Red #40,gelatin, glycerin, polyethylene glycol, povidone, propylene glycol, purified water,sorbitol specialand white edible ink

Questions or comments?

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Ingredients and appearance - Product information

Tussin dm cough and chest congestion capsule, liquid filled- Dextromethorphan hydrobromide, guaifenesin

Product information

Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC: 51013-166
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Dextromethorphan hydrobromide ( UNII: 9D2RTI9KYH)( Dextromethorphan - UNII: 7355X3ROTS ) 10 mgin 1
Guaifenesin ( UNII: 495W7451VQ)( Guaifenesin - UNII: 495W7451VQ ) 200 mgin 1

Inactive Ingredients

Ingredient Name Code
Fd&c red no. 40 ( UNII: WZB9127XOA)
Gelatin ( UNII: 2G86QN327L)
Glycerin ( UNII: PDC6A3C0OX)
Polyethylene glycols ( UNII: 3WJQ0SDW1A)
Povidone ( UNII: FZ989GH94E)
Propylene glycol ( UNII: 6DC9Q167V3)
Water ( UNII: 059QF0KO0R)
Sorbitol ( UNII: 506T60A25R)

Product Characteristics

Color red (clear) Shape capsule (oblong)
Size 20 mm Score 1
Imprint Code PC37

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
OTC monograph final part341 USA

Labeler - PuraCap Pharmaceutical LLC( 962106329)


Name ID/FEI Business Operations
PuraCap Pharmaceutical LLC 962106329 manufacture( 51013-166), analysis( 51013-166)

Principal display panel

Tussin DM Cough & Chest Congestion

NDC 51013-166-08

*Compare to the active ingredients in Robitussin ®Maximum Strength Cough Plus Chest Congestion DM