FDA Label for Conex
View Indications, Usage & Precautions
Conex Product Label
The following document was submitted to the FDA by the labeler of this product Llorens Pharmaceutical International Division. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Active Ingredient
Active Ingredients (in each 5 mL tsp.)
Dexbrompheniramine Maleate, USP .......... 2 mg .................... Antihistamine
Pseudoephedrine HCL, USP ............ 60 mg ...................... Nasal Decongestant
Otc - Purpose
Antihistamine
Nasal Decongestant
Indications & Usage
Uses
- Temporarily relieves nasal congestion due to the common cold, hay fever or other upper repiratory allergies
- helps decongest sinus opening and sinus passages
- reduces swelling of nasal passages, 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
- ithy and watery eyes
Warnings
Warnings:
- Do not use ifyou 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.
Otc - Do Not Use
Ask a doctor before use if you aretaking sedatives or tranquilizers.
Ask a doctor before use if you have
- heart disease
- high blood pressure
- thyroid disese
- diabetes
- difficulty in urination due to the enlargement of the prostate gland.
- do not exceed the recommended dosage
- excitability may occur, especially in children
- drowsiness may occur
- avoid alcoholic beverages
- alcohol, sedatives and tranquilizers may increase drowsiness
- use caution when driving a motor vehicle or operating machinery
- nervousness, dizziness or sleeplessness occur
- symptoms do not improve within 7 days or occur with a fever.
When using this product
Stop use and ask a doctor if
Otc - Keep Out Of Reach Of Children
Keep out of the reach of children.In case of overdose, get medical help or contact a Poison Control Center right away.
Otc - Pregnancy Or Breast Feeding
If pregnant or breast-feeding,ask a Health Professional before use.
Dosage & Administration
Directions:Do not exceed more than 4 doses in any 24-hour period or as directed by a doctor.
| Age | Dose |
| Adults and children 12 years of age and over | take two teaspoonfuls (10 mL) every 4 to 6 hours |
| Children under 12 years of age | Ask a doctor |
Inactive Ingredient
Inactive Ingredients: citric acid, flavor, glycerine, menthol, methylparaben, propylene glycol, propylparaben, purified water, sodium citrate and sucralose
Otc - Questions
Questions or Comments? 1-866-595-5598
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