Acticon®

Drug Facts

Composition & Product

Active Ingredients

Dexbrompheniramine (2 mg) Pseudoephedrine (60 mg)

Inactive Ingredients

Magnesium Stearate Microcrystalline Cellulose Sodium Starch Glycolate Type A

Identifiers & Packaging

Marketing Status

OTC MONOGRAPH DRUG Active Since 2015-08-13

Medication Information

Purpose

Antihistamine

Nasal Decongestant

Description

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

Uses

Temporarily relieves these symptoms due to the common cold, hay fever (allergic rhinitis) or other upper respiratory allergies:

• runny nose • sneezing

• itching of the nose or throat

• itchy, watery eyes

• nasal congestion

• reduces swelling of nasal passages

Section 42229-5

Contains the same active ingredients as Conex ^® Tablets*

Manufactured in USA with imported ingredients for ActiPharma, LLC. San Juan, PR 00917. www.actipharma.net

*Conex^® Tablets is a registered trademark of Llorens Pharmaceutical Corp. This product is not manufactured, distributed or marketed by Llorens Pharmaceutical Corp.

Tamper evident by foil seal under cap.

Do not use if foil seal is broken or missing.

Manufactured for:

ActiPharma

COMMITTED TO HEALTH AND WELL-BEING

WWW.ACTIPHARMA.NET

San Juan, PR 00917

Section 50565-1

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

Warnings

Do not exceed recommended dosage.

Do not use

• 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 mellitus

• 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

• 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.

Packaging

Directions

Do not exceed recommended dosage.

Adults and children 12 years of age and over:	1 tablet every 4 to 6 hours not to exceed 4 tablets in 24 hours or as directed by a doctor
Children 6 to under 12 years of age:	1/2 tablet every 4 to 6 hours not to exceed 2 tablets in 24 hours or as directed by a doctor
Children under 6 years of age	Consult a doctor

Drug Facts

Other Information

Store at 15°-30°C (59°-86°F) [see USP Controlled Room Temperature].

Inactive Ingredients

Magnesium stearate, microcrystalline cellulose, sodium starch glycolate

Questions Or Comments?

call weekdays from 8AM to 4PM AST at 1.787.608.0882

Active Ingredients (in Each Tablet)

Dexbrompheniramine Maleate, USP 2 mg

Pseudoephedrine HCl, USP 60 mg

Structured Label Content

Uses

Temporarily relieves these symptoms due to the common cold, hay fever (allergic rhinitis) or other upper respiratory allergies:

• runny nose • sneezing

• itching of the nose or throat

• itchy, watery eyes

• nasal congestion

• reduces swelling of nasal passages

Section 42229-5 (42229-5)

Contains the same active ingredients as Conex ^® Tablets*

Manufactured in USA with imported ingredients for ActiPharma, LLC. San Juan, PR 00917. www.actipharma.net

*Conex^® Tablets is a registered trademark of Llorens Pharmaceutical Corp. This product is not manufactured, distributed or marketed by Llorens Pharmaceutical Corp.

Tamper evident by foil seal under cap.

Do not use if foil seal is broken or missing.

Manufactured for:

ActiPharma

COMMITTED TO HEALTH AND WELL-BEING

WWW.ACTIPHARMA.NET

San Juan, PR 00917

Section 50565-1 (50565-1)

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

Purpose

Antihistamine

Nasal Decongestant

Warnings

Do not exceed recommended dosage.

Do not use

• 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 mellitus

• 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

• 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.

Packaging

Directions

Do not exceed recommended dosage.

Adults and children 12 years of age and over:	1 tablet every 4 to 6 hours not to exceed 4 tablets in 24 hours or as directed by a doctor
Children 6 to under 12 years of age:	1/2 tablet every 4 to 6 hours not to exceed 2 tablets in 24 hours or as directed by a doctor
Children under 6 years of age	Consult a doctor

Drug Facts

Other Information (Other information)

Store at 15°-30°C (59°-86°F) [see USP Controlled Room Temperature].

Inactive Ingredients (Inactive ingredients)

Magnesium stearate, microcrystalline cellulose, sodium starch glycolate

Questions Or Comments? (Questions or Comments?)

call weekdays from 8AM to 4PM AST at 1.787.608.0882

Active Ingredients (in Each Tablet) (Active ingredients (in each tablet))

Dexbrompheniramine Maleate, USP 2 mg

Pseudoephedrine HCl, USP 60 mg

Advanced Ingredient Data

[{"name": "DEXBROMPHENIRAMINE", "unii": "75T64B71RP", "classCode": "ACTIB", "strengthNumerator": "2", "strengthDenominator": "1", "strengthNumeratorUnit": "mg", "strengthDenominatorUnit": "1"}, {"name": "PSEUDOEPHEDRINE", "unii": "7CUC9DDI9F", "classCode": "ACTIB", "strengthNumerator": "60", "strengthDenominator": "1", "strengthNumeratorUnit": "mg", "strengthDenominatorUnit": "1"}, {"name": "MAGNESIUM STEARATE", "unii": "70097M6I30", "classCode": "IACT", "strengthNumerator": "", "strengthDenominator": "", "strengthNumeratorUnit": "", "strengthDenominatorUnit": ""}, {"name": "MICROCRYSTALLINE CELLULOSE", "unii": "OP1R32D61U", "classCode": "IACT", "strengthNumerator": "", "strengthDenominator": "", "strengthNumeratorUnit": "", "strengthDenominatorUnit": ""}, {"name": "SODIUM STARCH GLYCOLATE TYPE A", "unii": "H8AV0SQX4D", "classCode": "IACT", "strengthNumerator": "", "strengthDenominator": "", "strengthNumeratorUnit": "", "strengthDenominatorUnit": ""}]

Raw Label Data

All Sections (JSON)

{"Uses": "Temporarily relieves these symptoms due to the common cold, hay fever (allergic rhinitis) or other upper respiratory allergies: • runny nose • sneezing • itching of the nose or throat • itchy, watery eyes • nasal congestion • reduces swelling of nasal passages", "42229-5": "Contains the same active ingredients as Conex ® Tablets* Manufactured in USA with imported ingredients for ActiPharma, LLC. San Juan, PR 00917. www.actipharma.net *Conex ® Tablets is a registered trademark of Llorens Pharmaceutical Corp. This product is not manufactured, distributed or marketed by Llorens Pharmaceutical Corp. Tamper evident by foil seal under cap. Do not use if foil seal is broken or missing. Manufactured for: ActiPharma COMMITTED TO HEALTH AND WELL-BEING WWW.ACTIPHARMA.NET San Juan, PR 00917", "50565-1": "Keep out of reach of children. In case of accidental overdose, seek professional help or contact a Poison Control Center immediately.", "Purpose": "Antihistamine Nasal Decongestant", "Warnings": "Do not exceed recommended dosage. Do not use • 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 mellitus • 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 • 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.", "Directions": "Do not exceed recommended dosage. Adults and children 12 years of age and over: 1 tablet every 4 to 6 hours not to exceed 4 tablets in 24 hours or as directed by a doctor Children 6 to under 12 years of age: 1/2 tablet every 4 to 6 hours not to exceed 2 tablets in 24 hours or as directed by a doctor Children under 6 years of age Consult a doctor", "Other information": "Store at 15°-30°C (59°-86°F) [see USP Controlled Room Temperature].", "Inactive ingredients": "Magnesium stearate, microcrystalline cellulose, sodium starch glycolate", "Questions or Comments?": "call weekdays from 8AM to 4PM AST at 1.787.608.0882", "Active ingredients (in each tablet)": "Dexbrompheniramine Maleate, USP 2 mg Pseudoephedrine HCl, USP 60 mg"}

Drug Facts

Composition & Product

Identifiers & Packaging

Medication Information

Structured Label Content

Advanced Ingredient Data

Raw Label Data

Additional Information