Label: ACTINEL DM PEDIATRIC- dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride 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 5 mg

    Guaifenesin 75 mg

    Phenylephrine HCl 2.5 mg

  • Purposes

    Cough suppressant

    Expectorant

    Nasal decongestant

  • Uses

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

    • temporarily relieves:
      • nasal congestion due to the common cold
      • cough due to minor throat and bronchial irritation associated with a cold or inhaled irritants

  • Warnings

    Do not use in a child who is 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 child's prescription drug contains an MAOI, ask a doctor or pharmacist before giving this product.

    Ask a doctor before use if your child has
    • heart disease • high blood pressure • thyroid disease 
    • diabetes • cough accompanied by excessive phlegm (mucus) 
    • persistent or chronic cough such occurs with asthma

    When using this product
    • do not exceed recommended dosage

    Stop use and ask a doctor if
    • your child gets nervous, dizzy, or sleepless 
    • symptoms do not improve within 7 days or are accompanied by fever 
    • 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.

    Keep out of reach of children. In case of accidental overdose, seek professional assistance or contact a poison control center immediately.

  • Directions

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

    • mL = milliliter, tsp = teaspoon

    children 6 to under 12 years of age 10 mL (2 tsp) every 4 hours
    children 2 to under 6 years of age 5 mL (1 tsp) every 4 hours
    children under 2 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, glycerin, methylparaben, propylene glycol, propylparaben, purified water, sodium citrate, sucralose

  • Questions or comments?

    1.787.608.0882​

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

    Call weekdays from 8AM to 4PM AST

  • SPL UNCLASSIFIED SECTION

    Alcohol, Dye & Sugar FREE

    Contains the same active ingredients as Tusnel​®​ DM Pediatric*

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

    Manufactured for Actipharma
    San Juan, PR 00917.

    Manufactured in USA with imported ingredients​

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

  • Packaging

    ACTINEL​ DM Pediatric

  • INGREDIENTS AND APPEARANCE
    ACTINEL DM PEDIATRIC 
    dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63102-130
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE5 mg  in 5 mL
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN75 mg  in 5 mL
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE2.5 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
    FlavorSTRAWBERRY (Strawberry Banana) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63102-130-16473 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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