Label: GOOD SENSE TUSSIN CF MAX- dextromethorphan hydrobromide, guaifenesin and phenylephrine hydrochloride liquid

  • NDC Code(s): 0113-0296-26, 0113-0296-34
  • Packager: L. Perrigo Company
  • 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 05/14

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

  • Active ingredient (in each 5 mL tsp)

    Dextromethorphan HBr, USP 10 mg

    Guaifenesin, USP 200 mg

    Phenylephrine HCl, USP 5 mg

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  • Purposes

    Cough suppressant

    Expectorant

    Nasal decongestant

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  • Uses

    helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes
    temporarily relieves these symptoms occurring with a cold:
    nasal congestion
    cough due to minor throat and bronchial irritation
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  • 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

    heart disease
    high blood pressure
    thyroid disease
    diabetes
    trouble urinating due to an enlarged prostate gland
    cough that occurs with too much phlegm (mucus)

    cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema

    When using this product

    do not use more than directed

    Stop use and ask a doctor if

    you get nervous, dizzy, or sleepless
    symptoms do not get better within 7 days or are accompanied by fever
    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)

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  • Directions

    shake well before using
    do not take more than 6 doses in any 24-hour period
    use only with enclosed measuring cup. Do not use with any other device.
    this adult product is not intended for use in children under 12 years of age

    age

    dose

    adults and children 12 years and over

    2 teaspoons (tsp) every 4 hours

    children under 12 years

    do not use

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  • Other information

    each teaspoon contains: sodium 4 mg
    store at 20°-25°C (68°-77°F)
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  • Inactive ingredients

    anhydrous citric acid, FD&C red no. 40, flavor, glycerin, menthol, polyethylene glycol, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol solution, sucralose, xanthan gum

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  • Questions or comments?

    1-800-719-9260

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  • Package/Label Principal Display Panel

    Non-Drowsy

    Tussin

    CF MAX

    Multi-Symptom Cold

    Cough Suppressant (Dextromethorphan HBr)

    Expectorant (Guaifenesin)

    Nasal Decongestant (Phenylephrine HCl)

    Maximum Strength

    Relieves:

    Nasal Congestion

    Coughs

    Mucus

    Adult

    For Ages 12 & Over

    Alcohol Free

    Compare to active ingredients of Robitussin® Maximum Strength Multi-Symptom Cold

    4 FL OZ (118 mL)

    Tussin CF MAX Carton
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  • INGREDIENTS AND APPEARANCE
    GOOD SENSE TUSSIN  CF MAX
    dextromethorphan hbr, guaifenesin, phenylephrine hcl liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:0113-0296
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    DEXTROMETHORPHAN HYDROBROMIDE (DEXTROMETHORPHAN) DEXTROMETHORPHAN HYDROBROMIDE 10 mg  in 5 mL
    GUAIFENESIN (GUAIFENESIN) GUAIFENESIN 200 mg  in 5 mL
    PHENYLEPHRINE HYDROCHLORIDE (PHENYLEPHRINE) PHENYLEPHRINE HYDROCHLORIDE 5 mg  in 5 mL
    Inactive Ingredients
    Ingredient Name Strength
    ANHYDROUS CITRIC ACID  
    FD&C RED NO. 40  
    GLYCERIN  
    MENTHOL  
    POLYETHYLENE GLYCOLS  
    PROPYLENE GLYCOL  
    WATER  
    SODIUM BENZOATE  
    SODIUM CITRATE  
    SORBITOL  
    SUCRALOSE  
    XANTHAN GUM  
    Product Characteristics
    Color RED Score     
    Shape Size
    Flavor FRUIT PUNCH, MENTHOL Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0113-0296-26 1 in 1 CARTON
    1 118 mL in 1 BOTTLE
    2 NDC:0113-0296-34 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 01/11/2013
    Labeler - L. Perrigo Company (006013346)
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