ACTICON- dexbrompheniramine maleate, pseudoephedrine hydrochloride solution 
ACTIPHARMA, INC

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.

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NEW ACTICON®Cold & Allergy Oral Solution

Drug Facts

Active Ingredients 
(in each 5 mL tsp)

Dexbrompheniramine Maleate, USP 2 mg 
Pseudoephedrine HCl, USP 60 mg

Purpose

Antihistamine
Nasal Decongestant

Uses

• Temporarily relieves these symptoms due to the common cold, hay fever (allergic rhinitis) or other upper 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 • if 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.

                                      AGE                                  DOSE
 Adults and children 12 years of age and over 1 teaspoonful (5 ml) every 4-6 hours

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.

Contains the same active ingredients as Conex®*

Cherry Flavor

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

Manufactured in the USA for ActiPharma, Inc. San Juan, PR 00917. Tel: 787.608.0882. Rev. 5/21
* Conex® is a registered trademark of Llorens Pharmaceutical Corp. This product is not manufactured, distributed or marketed by Llorens Pharmaceutical Corp.

Packaging

cold & allergy

ACTICON 
dexbrompheniramine maleate, pseudoephedrine hydrochloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63102-108
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXBROMPHENIRAMINE MALEATE (UNII: BPA9UT29BS) (DEXBROMPHENIRAMINE - UNII:75T64B71RP) DEXBROMPHENIRAMINE MALEATE2 mg  in 5 mL
PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F) PSEUDOEPHEDRINE HYDROCHLORIDE60 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:63102-108-16474 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/15/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34102/15/2022
Labeler - ACTIPHARMA, INC (079340948)

Revised: 2/2022
Document Id: 1e3396fc-76ce-400e-84c8-ee47ceda84c9
Set id: aea0335d-75e6-4a90-86a5-f197cf024a11
Version: 1
Effective Time: 20220210
 
ACTIPHARMA, INC