Label: CHEST CONGESTION AND COUGH RELIEF DM- dextromethorphan hbr, guaifenesin capsule, liquid filled

  • NDC Code(s): 55301-601-02
  • Packager: ARMY AND AIR FORCE EXCHANGE SERVICE
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 19, 2025

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  • ACTIVE INGREDIENT

    Drug Facts

    Active ingredients (per softgel)
    Dextromethorphan HBr 10 mg
    Guaifenesin 200 mg

  • PURPOSE

    Purposes
    Dextromethorphan HBr ..........................Cough Suppressant
    Guaifenesin       ....................................Expectorant

  • INDICATIONS & USAGE

    Uses
    ■ helps loosen phlegm (mucus) and thin broochial secretions to make cough more
       productlve
    ■ temporarily relieves cough due to minor throat and bronchial irritation as may
      occur with a cold

  • WARNINGS

    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 two 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 DOCTOR

    Ask a doctor before use if you have
    ■ cough that occurs with too much phlegm (mucus)
    ■ cough that lasts or is chronic such as occurs with smoking, asthma, chronic
       bronchitis or emphysema

  • STOP USE

    Stop use and ask a doctor ifcough lasts more than 7 days, comes back, or is
    accompanied by fever, rash, or persistent headache. These could be signs of a
    serious condition.

  • PREGNANCY OR BREAST FEEDING

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

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

    In case of overdose, get medical help or contact a
    Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions
    ■ Do not take more than 12 softgels in any 24·hour period
    ■ This product is nol lntended for use in children under 12 years
    ■ Adults & children 12 years and over - 2 softgels every 4 hours
    ■ Children under 12 years of age - do not use

  • OTHER SAFETY INFORMATION

    Other information
    ■ Store at room temperature
    ■ Avoid excessive heat above 40'C (104'F)

  • INACTIVE INGREDIENT

    Inactive ingredients
    FD&C Red # 40, Gelatin, Glycerin, Polyethylene glycol, Povidone, Propylene
    glycol, Purified water, Sorbitol sorbllan solulion, Titanium dioxide

  • QUESTIONS

    Questions? 1-877-798-5944

  • Product Label: exchange select Chest Congestion & Cough Relief DM

    55301-601 Box

    exchange select

    Chest Congestion

    & Cough Relief DM

    20 Softgels  Ages 12+

    Manufactured For Your Military Exchange

    By AptaPharma Inc.,

    1533 Union Avenue, Pennsauken, NJ 08110

    1-877-798-5944

    aptapharma.com

    res

  • INGREDIENTS AND APPEARANCE
    CHEST CONGESTION AND COUGH RELIEF DM 
    dextromethorphan hbr, guaifenesin capsule, liquid filled
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55301-601
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN200 mg
    Inactive Ingredients
    Ingredient NameStrength
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GELATIN (UNII: 2G86QN327L)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POVIDONE (UNII: FZ989GH94E)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SORBITOL (UNII: 506T60A25R)  
    SORBITAN (UNII: 6O92ICV9RU)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorredScoreno score
    ShapeOVALSize20mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55301-601-022 in 1 CARTON01/01/2025
    110 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01201/01/2025
    Labeler - ARMY AND AIR FORCE EXCHANGE SERVICE (001695568)
    Registrant - AptaPharma Inc. (790523323)
    Establishment
    NameAddressID/FEIBusiness Operations
    AptaPharma Inc.790523323manufacture(55301-601)
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