Label: DM MAX- dextromethorphan hbr, guaifenesin, phenylephrine hcl solution

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

Drug Label Information

Updated January 1, 2025

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

  • ACTIVE INGREDIENT

    Drug Facts

    Active ingredients

    (in each 20 mL)

    Dextromethorphan HBr 20 mg
    Guaifenesin 400 mg

  • PURPOSE

    Purpose

    Dextromethorphan HBr ..........Cough suppressant
    Guaifenesin ...........................Expectorant

  • INDICATIONS & USAGE

    Uses

    ■ helps loosen phlegm (mucus)
    and thin bronchial secretions
    to drain bronchial tubes
    ■ Temporarily relieves these symptoms ocurring with a cold:
          ■ cough due to minor throat and bronchial irritation

  • WARNINGS

    Warnings

    Do not use: ■ for children under 12 years of age
    ■ 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 lasts or is chronic
    such as occurs with smoking, asthma,
    chronic bronchitis or emphysema
    ■ cough that occurs with too much phlegm (mucus)

  • WHEN USING

    When using this product, do not use
    more than directed

  • STOP USE

    Stop use and ask a doctor if

    ■ cough lasts for more than 7 days
    days comes back, or occurs with fever,
    rash or persistent headache.

    These could be signs of a serious condition.

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast feeding ask a health professional before use.

    In case of overdose, gel medical help or contact a
    Poison Control Genter rightaway.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. In case of overdose, get
    medical help or contact a Poison Control Center right
    away.

  • DOSAGE & ADMINISTRATION

    Directions
    ■ take only as recommended
    ■ use dosage cup
    ■ mL= milliliter
    ■ do not take more than 6 doses in any 24-hour period

    Age                                                                                  Dose                                                         

     Adults & children 12 years and older

     20 mL every 4 hours              

     Children under 12 years of age

     Do not use

  • OTHER SAFETY INFORMATION

    Other information
    Each 20 mL contains: sodium 12 mg
    ■ dosage cup provided
    ■ store between 15-30° C (59-86° F)
    ■ do not refrigerate

  • INACTIVE INGREDIENT

    Inactive ingredients

    anhydrous citric acid, dextrose

    D&C Blue #33, FD&C Red#40,

    flavors, glycerin, maltitol,

    propylene glycol, purified

    water, saccharin sodium,

    sodium benzoate, sucralose,

    xanthan gum

  • QUESTIONS

    Questions? Call weekdays from 9:30 AM to 4:30 PM EST at 1-877-798-5944

  • -----------

    Product Label: Best Choice® DM Max

    Best Choice®

    MAXIMUM STRENGTH

    DM Max

    6 FL OZ (177 mL)

    PROUDLY DISTRIBUTED BY:

    VALUE MERCHANDISERS, CO.

    5000 KANSAS AVE

    KANSAS CITY, KS 66106

    • This product is not manufactured or distributed by Reckitt Benckiser Inc.,
    distributor of Mucinex" FAST-MAX™ DM MAX®

    518 DM Max Botl

    518 DM Max Labl

    res

  • INGREDIENTS AND APPEARANCE
    DM MAX 
    dextromethorphan hbr, guaifenesin, phenylephrine hcl solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63941-518
    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
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    DEXTROSE (UNII: IY9XDZ35W2)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    MALTITOL (UNII: D65DG142WK)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    ColorredScore    
    ShapeSize
    FlavorCHERRYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63941-518-25177 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01201/01/2025
    Labeler - Best Choice (868703513)
    Registrant - AptaPharma Inc. (790523323)
    Establishment
    NameAddressID/FEIBusiness Operations
    AptaPharma Inc.790523323manufacture(63941-518)