Label: MUCINEX FAST-MAX KICKSTART SEVERE CONGESTION AND COUGH MAXIMUM STRENGTH- dextromethorphan hydrobromide, guaifenesin liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 22, 2024

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

  • Drug Facts

  • ACTIVE INGREDIENT

    Active ingredients
    (in each 20 mL)
    Dextromethorphan HBr 20 mg
    Guaifenesin 400 mg

  • Uses

    Uses


    ■ helps loosen phlegm (mucus) and thin
    bronchial secretions to rid the bronchial
    passageways of bothersome mucus and
    make coughs more productive
    ■ temporarily relieves:
    ■ cough due to minor throat and
    bronchial irritation as may occur with
    the common cold or inhaled irritants
    ■ the intensity of coughing
    ■ the impulse to cough to help you get
    to sleep

  • 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
    ■ persistent or chronic cough such as occurs
    with smoking, asthma, chronic bronchitis, or
    emphysema
    ■ cough that occurs with too much phlegm (mucus)

    When using this product do not use more
    than directed


    Stop use and ask a doctor if
    ■ cough lasts more than 7 days, comes back, or
    occurs with fever, rash, or headache that lasts.
    These could be signs of a serious condition.

  • Directions

    Directions
    ■ do not take more than 6 doses in any
    24-hour period
    ■ measure only with dosing cup provided
    ■ do not use dosing cup with other products
    ■ dose as follows or as directed by a doctor
    ■ adults and children 12 years of age and over:
    20 mL in dosing cup provided every 4 hours
    ■ children under 12 years of age: do not use

  • OTHER SAFETY INFORMATION

    Other information
    ■ each 20 mL contains: sodium 9 mg
    ■ store at 20-25°C (68-77°F)
    ■ do not refrigerate

  • KEEP OUT OF REACH OF CHILDREN

    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.

  • INACTIVE INGREDIENT

    Inactive ingredients

    ammonium, glycyrrhizate, anhydrous citric acid, D&C yellow
    no. 10, edetate disodium, FD&C blue no. 1, flavor,
    glycerin (soy), propylene glycol, purified water,
    sodium benzoate, sorbitol, sucralose, trisodium
    citrate dihydrate*, xanthan gum
    *may contain this ingredient

  • QUESTIONS

    Questions?
    1-866-MUCINEX (1-866-682-4639)

  • PURPOSE

    Dextromethorphan HBr » Cough Suppressant
    Guaifenesin » Expectorant

  • PRINCIPAL DISPLAY PANEL

    NDC 72854-159-66

    Relieves Chest Congestion
    Controls Cough
    Thins& Loosens Mucus

    6 fl oz (180mL)

    MENTHOL FLAVORED LIQUID

    Dextromethorphan HBr » Cough Suppressant
    Guaifenesin » Expectorant

    Ages 12+

    Label

    Label

  • INGREDIENTS AND APPEARANCE
    MUCINEX FAST-MAX KICKSTART SEVERE CONGESTION AND COUGH  MAXIMUM STRENGTH
    dextromethorphan hydrobromide, guaifenesin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72854-159
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN400 mg
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE20 mg
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SORBITOL (UNII: 506T60A25R)  
    WATER (UNII: 059QF0KO0R)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Product Characteristics
    ColorgreenScore    
    ShapeSize
    FlavorMENTHOLImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72854-159-66180 in 1 BOTTLE; Type 0: Not a Combination Product08/15/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01208/15/2024
    Labeler - RB Health (US) LLC (081049410)