Label: MUCINEX FAST-MAX DM MAX AND MUCINEX FAST-MAX NIGHTTIME DM MAX VALUE PACK- dextromethorphan hbr, guaifenesin and triprolidine hcl kit

  • NDC Code(s): 63824-019-66, 72854-141-66, 72854-142-26
  • Packager: Reckitt Benckiser LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 4, 2026

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

  • ACTIVE INGREDIENT

    Active ingredients (in each 20 mL)

    Day:
    Dextromethorphan HBr 20 mg
    Guaifenesin 400 mg

    Night:

    Dextromethorphan HBr 20 mg
    Triprolidine HCl 2.5 mg

  • PURPOSE

    Purposes

    Day:
    Dextromethorphan HBr 20 mg.....................................Cough suppressant
    Guaifenesin 400 mg........................................................Expectorant

    Night:

    Dextromethorphan HBr 20 mg...............................................Cough suppressant
    Triprolidine HCl 2.5 mg....................................................................Antihistamine

  • INDICATIONS & USAGE

    Uses

    Day:
    ■ 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

    Night:

    ■ 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
    ■ runny nose
    ■ sneezing
    ■ itching of the nose or throat
    ■ itchy, watery eyes due to hay fever

  • WARNINGS

    Warnings

    Day:
    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.

    Night:

    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
    ■ glaucoma
    ■ trouble urinating due to an enlarged prostate gland
    ■ a breathing problem such as emphysema or chronic bronchitis
    ■ persistent or chronic cough such as occurs with smoking, asthma, or emphysema
    ■ cough that occurs with too much phlegm (mucus)


    Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers


    When using this product
    ■ do not use more than directed

    ■ excitability may occur, especially in children
    ■ marked drowsiness may occur
    ■ alcohol, sedatives, and tranquilizers may increase drowsiness
    ■ avoid alcoholic drinks
    ■ use caution when driving a motor vehicle or operating machinery


    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.

  • 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.

  • DOSAGE & ADMINISTRATION

    Directions

    Day:
    ■ 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

    Night:

    ■ do not take more than 4 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

    Day/Night:

    ■ each 20 mL contains: sodium 12 mg

    ■ store at 20-25°C (68-77°F)
    ■ do not refrigerate

  • INACTIVE INGREDIENT

    Inactive ingredients

    Day:
    ammonium glycyrrhizate, anhydrous citric acid, edetate disodium, FD&C red no. 40,
    flavor, glycerin (soy), propyl gallate, propylene glycol, purified water, sodium benzoate,
    sorbitol, sucralose, trisodium citrate dihydrate*, xanthan gum
    *may contain this ingredient

    Night:

    ammonium glycyrrhizate, anhydrous citric acid,
    carmine, edetate disodium, flavor, glycerin
    (soy),maltodextrin, propylene glycol,
    purified water, sodium benzoate, sorbitol,
    sucralose, xanthan gum

  • QUESTIONS

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

  • PRINCIPAL DISPLAY PANEL

    Front of comboBack of Combo

    carton label

    full carton label

  • INGREDIENTS AND APPEARANCE
    MUCINEX FAST-MAX DM MAX AND MUCINEX FAST-MAX NIGHTTIME DM MAX VALUE PACK 
    dextromethorphan hbr, guaifenesin and triprolidine hcl kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72854-142
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72854-142-262 in 1 CARTON07/01/2026
    11 in 1 BOTTLE; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 BOTTLE 180 mL
    Part 21 BOTTLE 180 mL
    Part 1 of 2
    MUCINEX FAST-MAX  DM MAX
    dextromethorphan hydrobromide and guaifenesin solution
    Product Information
    Item Code (Source)NDC:63824-019
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE20 mg  in 20 mL
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN400 mg  in 20 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
    SORBITOL (UNII: 506T60A25R)  
    AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    WATER (UNII: 059QF0KO0R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYL GALLATE (UNII: 8D4SNN7V92)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Product Characteristics
    ColorredScore    
    ShapeSize
    FlavorCHERRYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63824-019-66180 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01207/18/2012
    Part 2 of 2
    MUCINEX FASTMAX NIGHTTIME DM MAX 
    dextromethorphan hydrobromide, triprolidine hydrochloride solution
    Product Information
    Item Code (Source)NDC:72854-141
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRIPROLIDINE HYDROCHLORIDE (UNII: YAN7R5L890) (TRIPROLIDINE - UNII:2L8T9S52QM) TRIPROLIDINE HYDROCHLORIDE2.5 mg  in 20 mL
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE20 mg  in 20 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    SORBITOL (UNII: 506T60A25R)  
    CARMINIC ACID (UNII: CID8Z8N95N)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    Product Characteristics
    ColorpurpleScore    
    ShapeSize
    FlavorCHERRY (ELDERBERRY AND CHERRY) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72854-141-661 in 1 CARTON
    1180 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01207/01/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01207/01/2026
    Labeler - Reckitt Benckiser LLC (094405024)