BIO-CNEX- dexbrompheniramine maleate, pseudoephedrine hcl liquid

BIO-CNEX by

Drug Labeling and Warnings

BIO-CNEX by is a Otc medication manufactured, distributed, or labeled by Advanced Generic Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients (in each 5 mL tsp.)                 Purpose

Dexbrompheniramine maleate 1 mg                            Antihistamine

Pseudoephedrine Hydrochloride 30 mg                         Nasal Decongestant

PURPOSE

Purpose

Antihistamine

Nasal Decongestant

WARNINGS

Warnings

DO not use If you are 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 you are taking a prescription drug that contains an MAOI, ask your doctor or pharmacist before taking this product.

Ask a doctor before use if you are taking sedative or tranquilizers.

Ask a doctore before use if you have

• heart disease
• high blood pressure
• thyroid disease
• diabetes
• glaucoma
• difficulty in urinations due to the enlargment of the prostate gland.

When using this product

• Do not exceed the recommended dosage
• excitability may occur, espicially in children
• drowsiness may occur
• avoid alcoholic beverages
• alcohol, sedatives and tranquilizers may increase drowsiness
• use cuation 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 occur with fever.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.In case of overdose, get medical help or contact a Poison Control Center right away

PREGNANCY OR BREAST FEEDING

If pregnant or breast-feeding,ask a Health Professional before use.

DOSAGE & ADMINISTRATION

Directions do not exceed 4 doses in 24 hours.

• adults and children12 years of age and over:

  take two teaspoonfuls (10 mL)

  every 4 to 6 hours

• children 6 to under12 years of age:

  take one teaspoonful (5 mL)

  every 4 to 6 hours

• children under 6 years of age:

  ask a doctor

INDICATIONS & USAGE

Uses

• Temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies
• helps decongest sinus opening and sinus passages
• reduces swelling of nasal pasages, shrinks swollen membranes, and temporarily restores freer breathing through the nose
• temporarily alleviates the following symptoms due to hay fever (allergic rhinitis)
• runny nose
• sneezing
• itching of the nose or throat
• itchy and watery eyes

INACTIVE INGREDIENT

Inactive ingredients Aspertame, cherry flavor, citric acid, glycerine, menthol, methylparaben, potsassium citrate, potassium sorbate, propylene glycol, propylparaben and purified water.

QUESTIONS

Questions or comments?

1-305-403-3788

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BIO-CNEX 
dexbrompheniramine maleate, pseudoephedrine hcl liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 45737-239
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXBROMPHENIRAMINE MALEATE (UNII: BPA9UT29BS) (DEXBROMPHENIRAMINE - UNII:75T64B71RP)	DEXBROMPHENIRAMINE MALEATE	1 mg  in 5 mL
PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F)	PSEUDOEPHEDRINE HYDROCHLORIDE	30 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
ASPARTAME (UNII: Z0H242BBR1)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
glycerin (UNII: PDC6A3C0OX)
MENTHOL (UNII: L7T10EIP3A)
METHYLPARABEN (UNII: A2I8C7HI9T)
POTASSIUM CITRATE (UNII: EE90ONI6FF)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color		Score
Shape		Size
Flavor	CHERRY (cherry flavor)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 45737-239-16	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	01/01/2017

Labeler - Advanced Generic Corporation (831762971)