Label: ACTICON PEDIATRIC- dexbrompheniramine maleate, pseudoephedrine hydrochloride solution

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

Drug Label Information

Updated July 17, 2025

If you are a consumer or patient please visit this version.

  • Drug Facts

  • Active ingredients (in each 5 mL tsp)

    Dexbrompheniramine Maleate, USP 1 mg

    Pseudoephedrine HCl, USP 30 mg

  • Purpose

    Antihistamine

    Nasal Decongestant

  • Uses

    • Temporarily relieves these symptoms due to the common cold, hay fever (allergic rhinitis) or other respiratory allergies:
    • relieves sinus congestion and pressure, helps decongest sinus openings and passages
    • restores freer breathing through the nose
    • runny nose • sneezing • itching of the nose or throat
    • itchy, watery eyes • nasal congestion

  • Warnings

    Do not exceed recommended dosage

    Do not use this product
    • 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
    • a breathing problem such as emphysema or chronic bronchitis • glaucoma • heart disease • high blood pressure • thyroid disease • diabetes 
    • difficulty in urination due to enlargement of the prostate gland

    Do not take this product if you are taking sedatives or tranquilizers, without first consulting your doctor.

    When using this product
    • excitability may occur, especially in children • may cause drowsiness • alcohol, sedatives and tranquilizers may increase drowsiness effect 
    • avoid alcoholic beverages • use caution when driving a motor vehicle or operating machinery

    Stop use and ask a doctor if
    • nervousness, dizziness, or sleeplessness occur • symptoms do not improve within 7 days or are accompanied by fever • new symptoms occur

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

    Keep out of reach of children. In case of accidental overdose, seek professional help or contact a Poison Control Center immediately.

  • Directions

    Do not exceed more than 4 doses in 24 hours, or as directed by a doctor.

    AGEDOSE
     Adults and children 12 years of age and over 2 teaspoonfuls (10 mL) every 4-6 hours
     Children 6 to under 12 years of age 1 teaspoonful (5 mL) every 4-6 hours
     Children under 6 years of age ask 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).

  • Inactive ingredients

    citric acid, flavor, methylparaben, potassium citrate, propylene glycol, propylparaben, purified water, sorbitol, sucralose.

  • Questions & Comments?

    call weekdays from 8 AM to 4 PM AST at 1.787.608.0882.

  • SPL UNCLASSIFIED SECTION

    Contains the same active ingredients as Conex® Pediatric*

    Alcohol FREE

    Dye FREE

    Sugar FREE

    Cherry Flavor

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

    Manufactured in the USA with imported ingredients for ActiPharma, LLC. San Juan, PR 00917. *Conex® is a registered trademark of Llorens Pharmaceutical Corp. This product is not manufactured, distributed or marketed by Llorens Pharmaceutical Corp.

  • Packaging

    ACTICON PEDIATRIC

  • INGREDIENTS AND APPEARANCE
    ACTICON PEDIATRIC 
    dexbrompheniramine maleate, pseudoephedrine hydrochloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63102-109
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXBROMPHENIRAMINE MALEATE (UNII: BPA9UT29BS) (DEXBROMPHENIRAMINE - UNII:75T64B71RP) DEXBROMPHENIRAMINE MALEATE1 mg  in 5 mL
    PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F) PSEUDOEPHEDRINE HYDROCHLORIDE30 mg  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    POTASSIUM CITRATE (UNII: EE90ONI6FF)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    SORBITOL (UNII: 506T60A25R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorCHERRYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63102-109-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product07/17/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01207/17/2025
    Labeler - ACTIPHARMA, LLC (079340948)