Label: COUGH RELIEF ADULT- dextromethorphan hbr liquid

  • NDC Code(s): 55910-309-04
  • Packager: Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated December 2, 2022

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  • Active ingredient (in each 5 mL)

    Dextromethorphan HBr 15 mg

  • Purpose

    Cough suppressant

  • Uses

    • temporarily relieves
      • cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants
      • 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

    • cough that occurs with too much phlegm (mucus)
    • chronic cough that lasts as occurs with smoking, asthma, or emphysema

    When using this product,

    do not use more than directed

    Stop use and ask a doctor if

    cough lasts more than 7 days, cough comes back, or  occurs by 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 (1-800-222-1222) right away.

  • Directions

    • take recommended dosage or as directed by a doctor
    • measure only with dosing cup provided. Do not use any other dosing device
    • keep dosing cup with product
    • shake well before using
    • mL=milliliter
    age dose 
     adults and children 12 years and over10 mL every 6-8 hours not to exceed 4 doses in 24 hours, 
    children 6 to 11 years of age5 mL every 6-8 hours not to exceed 4 doses in 24 hours
     children under 6 years of age do not use

  • Other information

    • each 5 mL contains: sodium 3 mg 
    • store between 20-25ºC (68-77ºF). Do not refrigerate.
  • Inactive ingredients

    anhydrous citric acid, disodium EDTA, FD&C yellow #6, flavor, glycerin, high fructose corn syrup, hydroxyethyl cellulose, polyethylene glycol, propylene glycol, purified water, sodium benzoate, sucralose, sucrose, xanthan gum

  • Questilons or comments?

    Call 1-888-309-9030

  • Principal Display Panel

    For Ages 6 Years and over

    Adult

    Cough Relief

    Dextromethorphan HBr 15 mg

    Cough suppressant

    Relieves:

    • Cough
    • Minor throat and bronchial irritation
    • impulse to cough

    6-8 Hour Relief

    Alcohol free

    FL OZ (mL)

    Orange flavor

    Dosing Cup Included

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

    DISTRIBUTED BY DOLGENCORP, LLC

    100 MISSION RIDGE

    GOODLETTSVILLE, TN 37072

  • Package Label

    Dextromethorphan HBr 15 mg

    DOLLAR GENERAL Adult Cough Relief

  • INGREDIENTS AND APPEARANCE
    COUGH RELIEF  ADULT
    dextromethorphan hbr liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55910-309
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE15 mg  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    WATER (UNII: 059QF0KO0R)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
    HYDROXYETHYL CELLULOSE (1500 MPA.S AT 1%) (UNII: L605B5892V)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    SUCROSE (UNII: C151H8M554)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorORANGEImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55910-309-041 in 1 BOX08/31/2015
    1118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34108/31/2015
    Labeler - Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) (068331990)
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