MUCUS RELIEF DM MAX MAXIMUM STRENGTH FAST ACTING (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)]

MUCUS RELIEF DM MAX MAXIMUM STRENGTH FAST ACTING (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)]
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NDC 55910-338-09
Set ID e51df3ae-977f-405f-b8e1-7f75fe4c5ef0
Category HUMAN OTC DRUG LABEL
Packager Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)
Generic Name
Product Class
Product Number
Application Number PART341
  • Active ingredients (in each 20 mL)

    Dextromethorphan HBr 20 mg

    Guaifenesin 400 mg

  • Purposes

    Cough suppressant

    Expectorant

  • Uses

    • helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of botherosme 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 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

    • 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.

  • 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
    • mL=milliliter
    • adults and children 12 years of age and older: 20 mL in dosing cup provided every 4 hours
    • children under 12 years of age: do not use

  • Other information

    • each 20 mL contains:potassium 6 mg,
    • each 20 mL  contains: sodium 13 mg
    • store between 20-25ºC (68-77ºF). Do not refrigerate
  • Inactive ingredients

    anhydrous citric acid, dextrose, D&C red #33, FD&C red #40, flavor, glycerin, methylparaben, potassium sorbate, propylene glycol, propylparaben, purified water, saccharin sodium, sodium hydroxide, sucralose, xanthan gum

  • Principal Display Panel

    Maximum Strength

    Fast Acting

    Mucus Relief DM Max

    Dextromethorphan HBr, 20 mg

     Cough Suppressant

    Guaifenesin, 400 mg

    Expectorant

    • Controls cough
    • relieves chest congestion
    • thins and loosens mucus
    • 4 hour dosing

    For ages 12 and over

    Compare to the active ingredients of Mucinex® Fast-Max® DM Max Maximum Strength*

    FL OZ (mL)

    DISTRIBUTED BY DOLGENCORP, LLC

    100 MISSION RIDGE

    GOODLETTSVILLE, TN 37072

    888-309-9030

    *This product is not manufactured or distributed by Reckitt Benckiser, distributor of Maximum Strength Mucinex® Fast-Max® DM Max Liquid.

    TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL AROUND OR UNDER CAP IS BROKEN OR MISSING.

  • Package Label

    Dextromethorphan HBr 20 mg, Guaifenesin 400 mg

    Dollar General Maximum Strength Mucus Relief DM Max

  • INGREDIENTS AND APPEARANCE
    MUCUS RELIEF DM MAX  MAXIMUM STRENGTH FAST ACTING
    dextromethorphan hbr, guaifenesin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55910-338
    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)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55910-338-09266 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/30/201512/30/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH FINALpart34104/30/201512/30/2021
    Labeler - Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) (068331990)

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