Label: ACTINEL DIABETIC- dextromethorphan hydrobromide, guaifenesin liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 15, 2026

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  • ​Drug Facts

  • ​Active ingredients (in each 5 mL teaspoonful)

    Dextromethorphan HBr 10 mg

    Guaifenesin 100 mg

  • ​Purposes

    Cough suppressant

    Expectorant

  • ​​Uses

    • helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive

    • temporarily relieves cough due to minor throat and bronchial irritation associated with a cold or inhaled irritants

  • ​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
    • cough is accompanied by excessive phlegm (mucus)
    • persistent or chronic cough such occurs with smoking, asthma, or emphysema

    ​When using this product
    • ​do not exceed recommended dosage

    ​Stop use and ask a doctor if
    • cough persists for more than 1 week, tends to recur, 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.

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

  • ​Directions

     • do not exceed 6 doses in any 24-hour period.

    • mL = milliliter, tsp = teaspoon

     adults and children 12 years of age and over 10 mL (2 tsp) every 4 hours
     children under 12 years of age consult a doctor

  • ​Other information

    • tamper evident feature: Do not use if inner seal is torn, cut, or opened

    • store at controlled room temperature 15° - 30°C (59° - 86°F)

    • avoid excessive heat or humidity

  • ​Inactive ingredients

    citric acid, flavor, methylparaben, propylene glycol, propylparaben, purified water, sodium citrate, sucralose

  • ​​Questions or comments?

    ​1.787.608.0082

    You may also report serious side effects to this phone number. 

    Call weekdays from 8AM to 4PM AST

  • SPL UNCLASSIFIED SECTION

    Alcohol FREE

    Dye FREE

    Sugar FREE

    Contains the same active ingredients as Tusnel® Diabetic* 

    ActiPharma
    COMMITTED TO HEALTH AND WELL-BEING
    WWW.ACTIPHARMA.NET

    Manufactured for ActiPharma
    San Juan, PR 00917

    Manufactured in USA with imported ingredients

    *Tusnel® Diabetic is a registered trademark of Llorens Pharmaceutical. This product is not manufactured, distributed or marketed by Llorens Pharmaceutical.

  • Packaging

    ACTINELDiabetic

  • INGREDIENTS AND APPEARANCE
    ACTINEL DIABETIC 
    dextromethorphan hydrobromide, guaifenesin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63102-140
    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
    Inactive Ingredients
    Ingredient NameStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    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
    FlavorSTRAWBERRY (Strawberry Banana Flavor) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63102-140-16473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/12/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01202/12/2026
    Labeler - ACTIPHARMA, LLC (079340948)
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