Label: MUCUS RELIEF DM HONEY AND BERRY FLAVOR- dextromethorphan hydrobromide and guaifenesin solution

  • NDC Code(s): 68163-605-06
  • Packager: RARITAN PHARMACEUTICALS INC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 29, 2025

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredients (in each 20 mL)Purposes

    Dextromethorphan HBr 20 mg

    Cough suppressant

    Guaifenesin 400 mg

    Expectorant

  • 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.

    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 at 1-800-222-1222.

  • 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 information

    • each 20 mL contains: sodium 8 mg
    • store at room temperature
    • do not refrigerate
  • Inactive ingredients

    citric acid, edetate disodium, flavors, glycerin, propylene glycol, purified water, sodium benzoate, sorbitol, sucralose, xanthan gum

  • Questions?

    1-866-467-2748

  • PRINCIPAL DISPLAY PANEL - 180 mL Bottle Label

    *Compare to the active ingredient in Maximum Strength Mucinex® Fast Max® DM Max Honey & Berry Flavor

    NDC 68163-605-06

    DRx Choice

    maximum Strength

    Mucus

    relief DM

    Dextromethorphan HBr – Cough Suppressant

    Guaifenesin – Expectorant

    • Controls Cough
    • Relieves Chest Congestion
    • Thins & Loosens Mucus
    • 4 Hour Dosing

    Honey& Berry Flavor

    Naturally and Artificially Flavored

    For Ages 12+

    6 FL OZ (180mL)

    Manufactured by:

    Raritan Pharmaceuticals

    8 Joanna Court

    East Brunswick,

    NJ 08816

    *This product is not manufactured or distributed by RB Health (US) the distributor of Maximum Strength Mucinex® Fast-Max® DM Max Honey & Berry Flavor

    DRx Choice Mucus Relief DM
  • INGREDIENTS AND APPEARANCE
    MUCUS RELIEF DM HONEY AND BERRY FLAVOR 
    dextromethorphan hydrobromide and guaifenesin solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68163-605
    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)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SORBITOL (UNII: 506T60A25R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorHONEYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68163-605-06180 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package04/21/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01204/21/2023
    Labeler - RARITAN PHARMACEUTICALS INC (127602287)