CONEX- dexbrompheniramine maleate, pseudoephedrine liquid 
Llorens Pharmaceutical International Division

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.

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DRUG FACTS

Active Ingredients (in each 5 mL tsp.)

Dexbrompheniramine Maleate, USP .......... 1 mg .................... Antihistamine

Pseudoephedrine HCL, USP ............ 30 mg ...................... Nasal Decongestant


Uses:


Warnings:

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

Ask a doctor before use if you have

When using this product
Stop use and ask a doctor if


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.

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 6 to under 12 years of age
 take one teaspoonful (5 mL) every 4 to 6 hours
 Children under 6 years of age
 ask a doctor

Other Information:

Inactive Ingredients: aspartame, cherry flavor, citric acid, glycerine, menthol, methylparaben, potassium citrate, potassium sorbate, propylene glycol, propylparaben and purified water.

Questions or Comments? 1-866-595-5598

ConexLabel

CONEX 
dexbrompheniramine maleate, pseudoephedrine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54859-802
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXBROMPHENIRAMINE MALEATE (UNII: BPA9UT29BS) (DEXBROMPHENIRAMINE - UNII:75T64B71RP) DEXBROMPHENIRAMINE MALEATE1 mg  in 5 mL
PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F) PSEUDOEPHEDRINE HYDROCHLORIDE30 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
ASPARTAME (UNII: Z0H242BBR1)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
GLYCERIN (UNII: PDC6A3C0OX)  
MENTHOL (UNII: L7T10EIP3A)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POTASSIUM CITRATE (UNII: EE90ONI6FF)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
Product Characteristics
Color    Score    
ShapeSize
FlavorCHERRY (cherry flavor) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54859-802-04118 mL in 1 BOTTLE; Type 0: Not a Combination Product11/01/2007
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34111/01/2007
Labeler - Llorens Pharmaceutical International Division (037342305)

Revised: 12/2020
Document Id: 0b13510e-96ea-481c-9013-ff68716ac472
Set id: c564e4f2-7d11-4f3e-aff2-35755fbe7d55
Version: 3
Effective Time: 20201223
 
Llorens Pharmaceutical International Division