Label: MAXIUM STRENGTH DM MAX- dextromethorphan hydrobromide, guaifenesin liquid

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

Drug Label Information

Updated December 23, 2024

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  • Drug FactsActive ingredients(in each 20 mL)

    Dextromethorphan HBr, USP 20 mg

    Guaifenesin 400 mg

  • Purpose

    Cough Suppressant

    Expectorant

  • 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.

  • Uses

    • helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes
    • temporaroly relieves these symptoms occuring with a cold:
    • cough due to minor throat and bronchial irritation
  • Warning

    DO NOT USE IF PRINTED SEAL UNDER CAP IS TORN OR MISSING.

    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 this product

    • do not use more than directed
  • Stop use and ask a doctor if

    • cough lasts for more than 7 days, comes back, or occurs with fever, rash or persistant headache. These could be signs of a serious condition.
  • If pregnany or breast feeding,

    ask a health professional before use.

  • Directions

    • take only as recommended
    • use dosage cup
    • mL= millilter
    • do not take more than 6 doses in any 24-hour period
     Age Dose
     Adults & children 12 years adn older 20 mL every 4 hours
     Children under 12 years of age Do not use

  • Other information

    • each 20 mL contains: sodium 12 mg
    • dosage cup provided
    • store between 15-30°C (59-86°F)
    • do not refrigerate
  • Inactive ingredients

    anhydrous citric acid, dextrose, D&C Red # 33, FD&C Red # 40, flavors, glycerin, maltitol, propylene glycol, purified water, saccharin sodium, sodium benzoate, sucralose, Xanthan gum

  • Questions?

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

  • DISCOUNT drug mart FOOD FAIR MAXIUM STRENGTH DM MAX product label

    *COMPARE TO THE ACTIVE INGREDIENTS IN MUCINEX® FAST-MAX™-DM MAX

    LF-010

    DISCOUNT

    drug mart

    FOOD FAIR

    MAXIUM STRENGTH DM MAX

    Dextromethorphan HBr/ Guaifenesin

    COUGH SUPPRESSANT/

    EXPECTORANT

    Controls Cough

    Thins & Loosens mucus

    Relieves Chest Congestion

    Adults

    For Ages 12 & Over

    6 FL OZ (177 mL)

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

    LB - 010 LOT: EXP:

    Peel Corner to Read Complete Drug Facts and Information

    SATISFACTION GUARANTEED
    IF DISSASIFIED , RETURN UNUSED PORTION AND PACKAGE TO STORE WHERE PURCHASED. IF UNABLE TO RETURN TO STORE, SEND REASON FOR DISSATISFACTION, NAME, ADDRESS AND EMPTY PACKAGE TO: DISCOUNT DRUG MART, 211 COMMERCE DRIVE, MEDINA, OHIO 44256

    AptaPharma 518 DPL

    AptaPharma 518 DPL1

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  • INGREDIENTS AND APPEARANCE
    MAXIUM STRENGTH DM MAX 
    dextromethorphan hydrobromide, guaifenesin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53943-518
    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)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53943-518-25117 mL in 1 BOTTLE; Type 0: Not a Combination Product12/10/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01212/10/2013
    Labeler - Discount Drug Mart (047741335)
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