Label: EQUALINE TUSSIN ADULT- dextromethorphan hydrobromide and guaifenesin liquid 

  • NDC Code(s): 41163-359-26, 41163-359-34
  • Packager: Supervalu Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 07/14

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

  • Active ingredients (in each 10 mL)

    Dextromethorphan HBr, USP 20 mg

    Guaifenesin, USP 200 mg

    Close
  • Purposes

    Cough suppressant

    Expectorant

    Close
  • 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
    Close
  • 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)

    Close
  • 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

    Close
  • Other information

    each 10 mL contains: sodium 6 mg
    store at 20-25°C (68-77°F)
    Close
  • 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

    Close
  • Questions or comments?

    1-877-932-7948

    Close
  • Principal Display Panel

    compare to Robitussin® Cough + Chest Congestion DM active ingredients

    adult

    tussin

    cough & chest congestion

    dextromethorphan HBr (cough suppressant)

    guaifenesin (expectorant)

    non-drowsy

    peak cold

    DM

    relieves:

    cough

    mucus

    for ages 12 & over

    ALCOHOL FREE

    4 FL OZ (118 mL)

    Tussin Carton Image 1
    Tussin Carton Image 2
    Close
  • INGREDIENTS AND APPEARANCE
    EQUALINE TUSSIN  ADULT
    dextromethorphan hbr, guaifenesin liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:41163-359
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    DEXTROMETHORPHAN HYDROBROMIDE (DEXTROMETHORPHAN) DEXTROMETHORPHAN HYDROBROMIDE 20 mg  in 10 mL
    GUAIFENESIN (GUAIFENESIN) GUAIFENESIN 200 mg  in 10 mL
    Inactive Ingredients
    Ingredient Name Strength
    ANHYDROUS CITRIC ACID  
    FD&C RED NO. 40  
    GLYCERIN  
    HIGH FRUCTOSE CORN SYRUP  
    PROPYLENE GLYCOL  
    WATER  
    SODIUM BENZOATE  
    MENTHOL  
    SODIUM CITRATE  
    SUCRALOSE  
    Product Characteristics
    Color RED (Orange-Red) Score     
    Shape Size
    Flavor CHERRY Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:41163-359-26 1 in 1 CARTON
    1 118 mL in 1 BOTTLE
    2 NDC:41163-359-34 1 in 1 CARTON
    2 237 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part341 08/24/2004
    Labeler - Supervalu Inc (006961411)
    Close