Label: CVS CHEST CONGESTION RELIEF DM- dextromethorphan hydrobromide / guaifenesin tablet

  • NDC Code(s): 69842-996-30, 69842-996-60
  • Packager: CVS Pharmacy, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 18, 2024

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  • ACTIVE INGREDIENT

    Active ingredient - (per tablet)

    Dextromethorphan Hydrobromide   20mg   Cough Suppressant
    Guaifenesin  400mg  Expectorant

  • ASK DOCTOR

    Ask doctor before use if you have

    persistent or chronic cough, such as occurs with smoking, asthma, bronchitis or emphysma

    cough is accompanied by excessive phlegm (mucous)

  • STOP USE

    Stop use and ask doctor if

    Symptoms are accompanied by fever, rash or persistent headache

    cough persists for more than 1 week or tends to recur

    A persistent cough may be a sign of a serious condition


  • DO NOT USE

    Do not use if you are now taking a prescription monoamine oxidase (inhiMor~MAIO)

    Certain drugs for depression, psychiatric or emotional conditioners or Parkinson's disease

    or for 2 weeks after stopping MAIO drug, If you do not know if your prescription drug contains

    an MAIO, ask your doctor or pharmacist before using this product.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children, In  ase of overdose, get medical help or contact a Poison Center immediately

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breastfeeding, ask a health professional before use.

  • INACTIVE INGREDIENT

    magnesium stearate, microcrystalline cellulose,
     colloidal silicon dioxide, (co) povidone, dicalcium
    phosphate, maltodextrin, sodium starch glycolate, stearic acid

  • DOSAGE & ADMINISTRATION

    Directions        
    • Adults and children 12 years of age and over:    
    take 1 tablet every 4 hours as needed    
    • Children 610 under 12 years of age: take 1/2 tablet every 4 hours as needed
    • Children under 6 years of age: consult a doctor    
    Do not exceed 6 doses in a 24 hour period or as directed by a doctor
    Other information store at 15'- 30' C (59'- 86'F)     Rev 10/U9 RCCF

  • INDICATIONS & USAGE

    Uses. temporarily relieves cough due to minor throat and bronchial irritation
    as may occur with a common cold • helps loosen phlegm (mucus) and thin
    bronchial secretions to rid the bronchial passageways of bothersome mucus
    • helps make coughs more productive

  • PURPOSE

    Purpose

    Cough Suppressant

    Expectorant

  • WARNINGS

    Do not use if you are now taking a prescription monoamine oxidase (inhiMor~MAIO)

    Certain drugs for depression, psychiatric or emotional conditioners or Parkinson's disease

    or for 2 weeks after stopping MAIO drug, If you do not know if your prescription drug contains

    an MAIO, ask your doctor or pharmacist before using this product.

  • PRINCIPAL DISPLAY PANEL

    package labelEnter section text here

  • INGREDIENTS AND APPEARANCE
    CVS CHEST CONGESTION RELIEF  DM
    dextromethorphan hydrobromide / guaifenesin tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-996
    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
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    COPOVIDONE (UNII: D9C330MD8B)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    ColorwhiteScore2 pieces
    ShapeOVALSize17mm
    FlavorImprint Code PH073
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69842-996-601 in 1 CARTON01/11/2010
    160 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2NDC:69842-996-301 in 1 CARTON01/28/2010
    230 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01212/07/2009
    Labeler - CVS Pharmacy, Inc. (062312574)
    Registrant - Reese Pharmaceutical Co (004172052)
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