ACTICON- dexbrompheniramine maleate, pseudoephedrine hydrochloride solution

ACTICON by

Drug Labeling and Warnings

ACTICON by is a Otc medication manufactured, distributed, or labeled by ACTIPHARMA, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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.

SPL UNCLASSIFIED SECTION

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

INGREDIENTS AND APPEARANCE

ACTICON 
dexbrompheniramine maleate, pseudoephedrine hydrochloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63102-108
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXBROMPHENIRAMINE MALEATE (UNII: BPA9UT29BS) (DEXBROMPHENIRAMINE - UNII:75T64B71RP)	DEXBROMPHENIRAMINE MALEATE	2 mg  in 5 mL
PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F)	PSEUDOEPHEDRINE HYDROCHLORIDE	60 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
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
Shape		Size
Flavor	CHERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63102-108-16	474 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/15/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	02/15/2022

Labeler - ACTIPHARMA, LLC (079340948)