MUCUS RELIEF DM EXTENDED RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR) TABLET [TARGET CORPORATION]

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MUCUS RELIEF DM EXTENDED RELEASE (GUAIFENESIN, DEXTROMETHORPHAN HBR) TABLET [TARGET CORPORATION]
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NDC 11673-833-20, 11673-833-40
Set ID e18db792-3f9b-4ae2-b27e-c15c3bf14fef
Category HUMAN OTC DRUG LABEL
Packager TARGET Corporation
Generic Name
Product Class
Product Number
Application Number ANDA209692
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  • Active ingredients (in each extended-release tablet)

    Dextromethorphan HBr 30 mg

    Guaifenesin 600 mg

  • Purpose

    Cough Suppressant

    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

    • for children under12 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

    • persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema
    • cough accompanied by 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 persistent headache. 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 (1-800-222-1222).

  • Directions

    • do not crush, chew, or break tablet
    • take with a full glass of water 
    • this product can be administered without regards for timing of meals
    • adults and children 12 years of age and older take 1 or 2 tablet every 12 hours; not more than 4 tablets in 24 hours
    • children under 12 years of age: do not use 
  • Other information

    store between 20º to 25ºC (68º to 77ºF)

  • Inactive ingredients

    carbomer, colloidal silicon dioxide, D&Cyellow #10 aluminum lake, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, povidone, talc

  • Questions?

    Call 1-800-910-6874

  • Principal Display Panel

    Compare to active ingredients in Mucinex® DM*

    Mucus Relief DM

    guaifenesin 600 mg

    expectorant

    dextromethorphan HBr 30 mg

    cough suppressant

    Controls Cough

    Thins and Loosens Mucus

    EXTENDED-RELEASE TABLETS

    *This product is not manufactured or distributed Reckitt Benckiser LLC, distributor of Mucinex® DM.

    TAMPER EVIDENT: DO NOT USE IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING.

    KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.

    Distributed by Target Corporation

    Minneapolis, MN 55403

    TM & ©2018 Target Brands, Inc.

  • Package Label

    Dextromethorphan HBr 30 mg, Guaifenesin 600 mg

    TARGET Mucus Relief DM

  • INGREDIENTS AND APPEARANCE
    MUCUS RELIEF DM EXTENDED RELEASE 
    guaifenesin, dextromethorphan hbr tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-833
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN600 mg
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE30 mg
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CARBOMER 934 (UNII: Z135WT9208)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    POVIDONE (UNII: FZ989GH94E)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    TALC (UNII: 7SEV7J4R1U)  
    Product Characteristics
    ColorYELLOWScoreno score
    ShapeOVALSize16mm
    FlavorImprint Code AN038
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-833-2020 in 1 CARTON01/01/2019
    11 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:11673-833-4040 in 1 CARTON01/01/2019
    21 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA20969201/01/2019
    Labeler - TARGET Corporation (006961700)
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