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

  • 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 11/13

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

  • Active ingredients

    Dextromethorphan HBr, USP 10 mg
    Guaifenesin, USP 100 mg
    Phenylephrine HCI, USP 5 mg

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  • Purpose

    Cough suppressant
    Expectorant
    Nasal decongestant

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  • Uses

    •helps loosen phlegm (mucus) and thin bronchial
    secretions to drain bronchial tubes

    temporarily relieves cough due to minor throat
    and bronchial irritation as may occur 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.

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  • Ask a doctor before use if you have

    • heart disease • diabetes
    • high blood pressure • thyroid disease
    • cough that lasts or is chronic such as occurs with
    smoking, asthma, chronic bronchitis or emphysema
    • cough that occurs with too much phlegm (mucus)
    • trouble urinating due to an enlarged prostate gland

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  • When using this product

    • do not use more than directed

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  • 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 more than 7 days, comes back, or is
    accompanied by fever, rash, or persistent headache.
    These could be signs of a serious condition.

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  • If pregnant or breast-feeding

    ask a health
    professional before use.

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  • Keep this and all drugs out of the reach of children.

    In case of accidental overdose, seek professional
    assistance or contact a Poison Control Center
    immediately.

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  • Directions

    • do not exceed 6 doses in a 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 teaspoonfuls (tsps) every 4 hours

    children under 12 years                          do not use



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  • Other information

     • alcohol-free• dosage cup provided
    • store at controlled room temperature

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  • Inactive ingredients

    citric acid, flavor, glycerin,
    lactic acid, menthol, propylene glycol, purified water,
    red 40, sodium benzoate, sorbitol, sucralose

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  • Principal Display Panel

    Rite Aid Pharmacy

    Compare to the Active Ingredients in Robitussin CF

    tussin cough and cold CF

    Dextromethorphan HBr, 10 mg

    guaifenesin, 100 mg

    Phenylephrine HCI, 5 mg

    cough suppressant, expectorant

    and nasal decongestant

    Non-Drowsy

    Alcohol Free

    Relieves- coughs, stuffy nose, chest congestion and mucus

    12 years and older

    4 FL Oz (118 mL)

    image of label

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  • INGREDIENTS AND APPEARANCE
    TUSSIN CF 
    robitussin cf liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:11822-0126
    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 100 mg  in 5 mL
    PHENYLEPHRINE HYDROCHLORIDE (PHENYLEPHRINE ) PHENYLEPHRINE HYDROCHLORIDE 5 mg  in 5 mL
    Inactive Ingredients
    Ingredient Name Strength
    CITRIC ACID MONOHYDRATE  
    GLYCERIN  
    LACTIC ACID  
    MENTHOL  
    PROPYLENE GLYCOL  
    SODIUM BENZOATE  
    SORBITOL  
    SUCRALOSE  
    FD&C Red No. 40  
    Product Characteristics
    Color      Score     
    Shape Size
    Flavor CHERRY (cherry) Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:11822-0126-4 118 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part341 11/13/2013
    Labeler - Rite Aid (014578892)
    Registrant - Aaron Industries Inc (101896231)
    Establishment
    Name Address ID/FEI Business Operations
    Aaron Industries Inc 101896231 manufacture(11822-0126), analysis(11822-0126)
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