Label: DESGEN DM- dextromethorphan hbr ,guaifenesin ,phenylephrine hcl solution

  • Category: HUMAN OTC DRUG LABEL

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 November 13, 2019

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  • Active ingredients (in each 5 mL tsp)

    Dextromethorphan HBr, 10 mg

    Guaifenesin, 100 mg

    Phenylephrine HCL, 5mg

  • Purpose

    Cough Suppressant

    Expectorant

    Nasal Decongestant

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children,In case of accidental overdose, get medical help or contact a Poison Control Center right away.

  • Uses

    • Suppresses cough due to minor throat and bronchial irritation associated with a cold or inhaled irritants.
    • helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passages of bothersome mucus, drain bronchial tubes, and make   coughs more productive
    • temporarily relieves nasal congestion due to a cold

  • 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
    • diabetes • heart disease • thyroid disease • high blood pressure • trouble urinating due to an enlarged prostate gland • cough that occurs with too much phlegm (mucus) • cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis or emphysema.

    When using this product do not use more than directed

    Stop use and ask a doctor if
    • you get nervous, dizzy, or sleepless
    • symptoms do not get better within 7 days or are accompanied by fever
    • coughs lasts more than 7 days, comes back, or is accompanied by fever, rash, or a persistent headache. These could be signs of a serious condition.

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

  • Directions

    Do not take more than 6 doses in any 24-hour period


    Every 4 hours
    Adult and Children 12 years of age and over           10 mL (2 tsp)
    Children 6 to under 12 years of age                         5 mL (1 tsp)
    Children under 6 years of age                                Consult physician

  • Inactive ingredients

    Citric Acid, flavor, glycerin, methylparaben, propylene glycol, propylparaben, purified water, sodium citrate and sucralose.

  • Other Information

    • Tamper evident feature: Do not use if inner seal is torn, broken or missing.
    • Store at controlled room temperature 15-30°C (59-86°F).
    • Avoid excessive heat or humidity

  • SPL UNCLASSIFIED SECTION

    Manufactured in the USA for Kramer Novis, San Juan, PR 00917, Tel (787) 767-2072 / www.kramernovis.com

  • Packaging

    image description

  • INGREDIENTS AND APPEARANCE
    DESGEN DM 
    dextromethorphan hbr ,guaifenesin ,phenylephrine hcl solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52083-646
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg  in 5 mL
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN100 mg  in 5 mL
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE5 mg  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorgrapeImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52083-646-16474 mL in 1 BOTTLE; Type 0: Not a Combination Product10/18/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34110/18/2014
    Labeler - Kramer Novis (090158395)
    Registrant - Kramer Novis (090158395)