Home > Pill Identifier > Dexbrompheniramine maleate 2 MG / Pseudoephedrine Hydrochloride 60 MG Oral Tablet

Pill Identifier Information of Dexbrompheniramine maleate 2 MG / Pseudoephedrine Hydrochloride 60 MG Oral Tablet

Drug Information

Dexbrompheniramine maleate 2 MG / Pseudoephedrine Hydrochloride 60 MG Oral Tablet

Imprint: LLORENS
Shape: C48345
Color: C48325
Ingredients: dexbrompheniramine; Pseudoephedrine
Size: 13.00
Score: 1
Rxtty: SCD
Author: LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION
Inactive Ingredients: CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS / CELLULOSE, MICROCRYSTALLINE / MAGNESIUM STEARATE / SODIUM STARCH GLYCOLATE TYPE B POTATO / WATER / FERRIC OXIDE RED / FERRIC OXIDE YELLOW / TITANIUM DIOXIDE>

Complete Information

  • ACTIVE INGREDIENT

    Active Ingredients (in each film coated tablet)                         Purpose

    Dexbrompheniramine Maleate, USP ................ 2 mg .................. Antihistamine

    Pseudeophedrine HCl, USP .................... 60 mg ..........................Nasal Decogestant

  • PURPOSE


    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

    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 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.

  • PREGNANCY OR BREAST FEEDING

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

  • DO NOT USE

    Do not useif 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.

  • DOSAGE & ADMINISTRATION

    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 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
  • INDICATIONS & USAGE

    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 INGREDIENT

    Inactive Ingredients:Dicalcium Phosphate, Microcrystalline Cellulose, Magnesium Stearate, Silicon dioxide

  • QUESTIONS

    Questions or Comments?                 1-866-595-5598

  • PRINCIPAL DISPLAY PANEL

    ConexAllergy702

  • INGREDIENTS AND APPEARANCE
    CONEX 
    dexbrompheniramine maleate, pseudoephedrine hcl tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54859-702
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXBROMPHENIRAMINE MALEATE (UNII: BPA9UT29BS) (DEXBROMPHENIRAMINE - UNII:75T64B71RP) DEXBROMPHENIRAMINE MALEATE2 mg
    PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F) PSEUDOEPHEDRINE HYDROCHLORIDE60 mg
    Inactive Ingredients
    Ingredient NameStrength
    CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    SODIUM STARCH GLYCOLATE TYPE B POTATO (UNII: 27NA468985)  
    WATER (UNII: 059QF0KO0R)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeOVALSize13mm
    FlavorImprint Code LLORENS
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54859-702-6060 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 DrugM01211/01/2007
    Labeler - LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION (037342305)
    Registrant - LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION (037342305)
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