Label: TUSSIN DM- dextromethorphan hbr, guaifenesin syrup

  • NDC Code(s): 70677-1185-1, 70677-1185-2
  • Packager: Strategic Sourcing Service, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 30, 2023

If you are a consumer or patient please visit this version.

  • Active ingredients (in each 20 mL)

    Dextromethorphan HBr, USP 20 mg

    Guaifenesin, USP 200 mg

  • Purposes

    Cough suppressant

    Expectorant

  • Uses

    • helps loosen phlegm (mucus) and thin bronchial secretions to:
    • drain bronchial tubes
    • make coughs more productive
    • rid bronchial passageways of bothersome mucus
    • temporarily relieve cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants
  • 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 1 week, comes back, or occurs with a fever, rash, or headache that lasts. 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

    • take every 4 hours
    • do not take more than 6 doses in 24 hours

    adults and children 12 years and over40 mL every 4 hours
    children under 12 yearsdo not use

  • Other information

    • store at 20º C to 25º C (68º F 77º F)
    • do not refrigerate
  • Inactive ingredients

    carboxymethylcellulose sodium, citric acid (anhydrous), flavor, glycerin, menthol, polyethylene glycol, propylene glycol, purified water, sodium benzoate, sodium citrate, sodium gluconate, sucralose, triacetin, xanthan gum

  • Questions or comments?

    Call (833) 358-6431 Monday - Friday 9 am - 7 pm EST

  • PRINCIPAL DISPLAY PANEL

    Principal Display PanelFoster & Thrive

    Adult

    Tussin DM

    Dextromethorphan HBr

    Guaifenesin

    Cough Suppressant

    Expectorant

    Cough & Chest Congestion DM

    Alcohol Free Dye Free Sugar Free

    • Relieves chest congestion
    • Controls cough
    • Thins & loosens mucus

    8 FL OZ (237 mL)

  • INGREDIENTS AND APPEARANCE
    TUSSIN DM 
    dextromethorphan hbr, guaifenesin syrup
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70677-1185
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN200 mg  in 20 mL
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE20 mg  in 20 mL
    Inactive Ingredients
    Ingredient NameStrength
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    MENTHOL (UNII: L7T10EIP3A)  
    WATER (UNII: 059QF0KO0R)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    TRIACETIN (UNII: XHX3C3X673)  
    SODIUM GLUCONATE (UNII: R6Q3791S76)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70677-1185-21 in 1 CARTON06/01/2023
    1236 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:70677-1185-11 in 1 CARTON06/01/2023
    2118 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01206/01/2023
    Labeler - Strategic Sourcing Service, LLC (116956644)
    Registrant - Weeks & Leo Co., Inc. (005290028)
    Establishment
    NameAddressID/FEIBusiness Operations
    Weeks & Leo Co., Inc.005290028manufacture(70677-1185)