Label: MUCUS RELIEF DM IMMEDIATE RELEASE- mucus relief dm tablet

  • NDC Code(s): 69168-432-06, 69168-432-07, 69168-432-26, 69168-432-30, view more
    69168-432-50, 69168-432-98
  • Packager: Allegiant Health
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 18, 2022

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  • Active ingredient(s)

    Dextromethorphan HBr 20mg
    Guaifenesin 400mg 

  • Purpose

    Cough suppressant
    Expectorant

  • Use(s)

    • 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

    • persistent or chronic cough such as
      occurs with smoking, asthma, chronic
      bronchitis or emphysema
    • cough accompanied by too much phlegm (mucus

    Ask a doctor or pharmacist before use if

    taking sedatives or tranquilizers

    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 persistent headache. These could be signs of a serious illness

    Pregnancy/Breastfeeding

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

    Keep out of reach of children

    In case of accidental overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    Adults and children 12 years and older: take 1 tablet every 4 hours with a full glass of water while symptoms persist. Do not exceed 6 doses in 24 hours.

    Children under 12 years of age: do not use

  • Other information

    • store at 25°C (77°F) excursions between 15°-30°C (59°-86°F)
    • keep in a dry place and do not expose to heat
    • do not use if imprinted safety seal under cap is broken or missing
    • You may report side effects to 1-888-952-0050
  • Inactive ingredients

    croscarmellose sodium, magnesium stearate, maltodextrin, microcrystalline cellulose, povidone, silicon dioxide, stearic acid

  • Questions

    Questions or comments?
    Call 1-888-952-0050
    Monday through Friday 9AM- 5PM EST.

  • Principal Display Panel

    Mucus Relief DM

    Mucus Relief DM


  • INGREDIENTS AND APPEARANCE
    MUCUS RELIEF DM  IMMEDIATE RELEASE
    mucus relief dm tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69168-432
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE20 mg
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN400 mg
    Inactive Ingredients
    Ingredient NameStrength
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    POVIDONE (UNII: FZ989GH94E)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    ColorwhiteScore2 pieces
    ShapeOVALSize16mm
    FlavorImprint Code AH432;bisect
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69168-432-98200 in 1 BOTTLE; Type 0: Not a Combination Product05/18/2022
    2NDC:69168-432-071 in 1 CARTON05/18/2022
    210 in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:69168-432-261 in 1 CARTON05/18/2022
    320 in 1 BOTTLE; Type 0: Not a Combination Product
    4NDC:69168-432-5050 in 1 BOTTLE; Type 0: Not a Combination Product06/08/2022
    5NDC:69168-432-06120 in 1 BOTTLE; Type 0: Not a Combination Product11/06/2023
    6NDC:69168-432-3030 in 1 BOTTLE; Type 0: Not a Combination Product11/06/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01205/18/2022
    Labeler - Allegiant Health (079501930)
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