ACTICON- dexbrompheniramine maleate, pseudoephedrine hydrochloride liquid 
ACTIPHARMA, INC.

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ACTICON Cold & Allergy oral solution

Drug Facts

Active Ingredients (in each 5 mL tsp)

Dexbrompheniramine Maleate, 1 mg

Pseudoephedrine HCl, 30 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 accompanined 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:

• Adults and children 12 years of age and over: Take 2 teaspoonfuls (10 mL) every 4-6 hours as needed, do not exceed 4 teaspoonfuls in 24 hours, or as directed by a doctor.

• Children 6-12 years: Take 1 teaspoonful (5 mL) every 4-6 hours as needed, do not exceed 2 teaspoonfuls in 24 hours, or as directed by a doctor.

• Children under 6 years of age: consult a doctor.

Other Information:

• Tamper Evident. Do not use if inner seal is torn, cut, or opened.

• Store at controlled room temperature 15°- 30ºC (59°- 86ºF)

Avoid excessive heat or humidity.

Inactive Ingredients:

citric acid, flavor, glycerin, methyl paraben, propylene glycol, propyl paraben, purified water, sodium citrate, sucralose

Contains the same active ingredients as Conex®*

Manufactured in the USA for ActiPharma, Inc.

Dorado, PR 00646. Tel: (787) 608-0882

* Conex® is a registered trademark of Llorens

Pharmaceutical Corp. This product is not manufactured, distributed or marketed by Llorens Pharmaceutical Corp.

Packaging

image description

ACTICON 
dexbrompheniramine maleate, pseudoephedrine hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63102-105
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)  
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
FlavorCHERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63102-105-16480 mL in 1 PACKAGE; Type 0: Not a Combination Product07/14/201601/31/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01207/14/201601/31/2023
Labeler - ACTIPHARMA, INC. (079340948)
Registrant - ACTIPHARMA, INC. (079340948)

Revised: 6/2024
 
ACTIPHARMA, INC.