Pill Identifier App

← See all Conex brands

Conex by LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION

Dosage form: tablet
Ingredients: DEXBROMPHENIRAMINE MALEATE 2mg, PSEUDOEPHEDRINE HYDROCHLORIDE 60mg
Labeler: LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION
NDC Code: 54859-702

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

DRUG FACTS

Active Ingredients (in each film coated tablet)                                               Purpose

Dexbrompheniramine Maleate, USP ................ 2 mg ................................... Antihistamine
Pseudeophedrine HCl, USP .................... 60 mg ......................................... Nasal Decogestant





Uses
  • Temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies
  • helps decongest sinus openings 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, itching and watery eyes.

Warnings:

Ask a doctor before you use if you are
  • taking sedatives or tranquilizers.
Ask your doctor before use if you have
  • heart disease
  • high blood pressure
  • thyroid disease
  • diabetes
  • glaucoma
  • difficulty in urination due to the enlargement of the prostate gland.
When using this product
  • 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
Stop use and ask doctor if
  • nervousness, dizziness or sleepiness occur
  • symptoms do not improve withing 7 days or occur with a fever

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

If pregnant or breast-feeding, ask a health professional before use.

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 MAOI;

ask your doctor or pharmacist before taking this product.

Directions; Do not exceed more than 4 tablets in any 24-hour period or as directed by a doctor.

 Adults and children
 12 years of age and over
 Take one tablet
 every 4 to 6 hours
 Children 6 to under
 12 years of age
 1/2 tablet
 every 4 to 6 hours
 Children under
 6 years of age
 Ask a doctor

Other Information: Store at controlled room temperature 20 - 25 degree celsius (68 - 77 degree fahrenheit); excursions permitted to

15 - 30 degree celsius ( 59 - 86 degree fahrenheit) [ See USP Controlled Room Temperature] Tamper evident by imprinted heat seal

under cap. Do not use if there is evidence of tampering.

Inactive Ingredients: Dicalcium Phosphate, Microcrystalline Cellulose, Magnesium Stearate, Sodium Starch Glycolate type B, Purified Water, Red iron Oxide, Yellow Iron Oxide, Titanium Dioxide.

Questions or Comments?                 1-866-595-5598

CONEX 
dexbrompheniramine maleate, pseudoephedrine hcl tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54859-702
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXBROMPHENIRAMINE MALEATE (DEXBROMPHENIRAMINE) DEXBROMPHENIRAMINE MALEATE2 mg
PSEUDOEPHEDRINE HYDROCHLORIDE (PSEUDOEPHEDRINE) PSEUDOEPHEDRINE HYDROCHLORIDE60 mg
Inactive Ingredients
Ingredient NameStrength
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS 
CELLULOSE, MICROCRYSTALLINE 
MAGNESIUM STEARATE 
SODIUM STARCH GLYCOLATE TYPE B POTATO 
WATER 
FERRIC OXIDE RED 
FERRIC OXIDE YELLOW 
TITANIUM DIOXIDE 
Product Characteristics
ColorwhiteScoreno score
ShapeOVALSize13mm
FlavorImprint CodeLLORENS
Contains    
Packaging
#Item CodePackage Description
1NDC:54859-702-6060 TABLET (TABLET) in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34111/01/2007
Labeler - LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION (037342305)
Registrant - LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION (037342305)

Revised: 06/2012
 
LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION

← See all Conex brands

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

Hide
(web4)