Home > Drugs A-Z > Pedia Relief

Pedia Relief (Major Pharmaceuticals, Inc)

Available Formats

Dosage Form Package Information Links
LIQUID 120 mL in 1 BOTTLE, PLASTIC (0904-5050-20) Label Information

Complete Pedia Relief Information


    Drug Facts


    Active ingredients (in each 2 TSP (10 mL)) Purposes
    Chlorpheniramine maleate, USP 2 mg Antihistamine
    Dextromethorphan HBr, USP 10 mg Cough suppressant
    Pseudoephedrine HCl, USP 30 mg Nasal decongestant

  • Uses

    temporarily relieves these symptoms of the common cold, hay fever or other upper respiratory allergies:

    • cough
    • nasal congestion
    • runny nose
    • sneezing
    • itching of the nose or throat
    • itchy, watery eyes

  • Warnings

    Do not use in a child who is 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 your child's prescription drug contains an MAOI, ask a doctor or pharmacist before giving this product.

    Ask a doctor before use if child has
    • a breathing problem such as chronic bronchitis
    • cough that occurs with too much phlegm (mucus)
    • chronic cough that lasts such as occurs with asthma
    • heart disease
    • thyroid disease
    • glaucoma
    • diabetes
    • high blood pressure

    Ask a doctor or pharmacist before use if the child is taking sedatives or tranquilizers

    When using this product
    • do not use more than directed
    • drowsiness may occur
    • excitability may occur, especially in children
    • sedatives and tranquilizers may increase drowsiness

    Stop use and ask a doctor if
    • cough lasts for more than 7 days, comes back, or occurs with fever, rash or persistent headache. A persistent cough may be a sign of a serious condition.
    • the child gets nervous, dizzy or sleepless
    • symptoms do not get better within 7 days or occur with fever

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

  • Directions

    • dose may be repeated every 6 hours
    • do not exceed 4 doses in a 24-hour period
    • use enclosed dosing cup only. Do not use with any other device.
    Children 6 to 11 years 2 TSP
    Children under 6 years Do not use

  • Other information

    • store at 20° - 25°C (68° - 77°F)

  • Inactive ingredients

    artificial cherry flavor, citric acid, FD&C red #40, glycerin, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol solution

  • Questions or comments?



    Distributed by:
    Major Pharmaceuticals
    17177 N Laurel Park Drive,
    Suite 233,
    Livonia, MI 48152

  • PRINCIPAL DISPLAY PANEL - 118 mL Bottle Label

    NDC 0904-5050-20



    Oral Solution

    Relief For

    • Coughs
    • Runny
    • Stuffy


    Cough Suppressant
    Nasal Decongestant

    4 FL OZ (118 mL)

    Principal Display Panel - 118 mL Bottle Label

    chlorpheniramine maleate and pseudoephedrine hydrochloride and dextromethorphan hydrobromide liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0904-5050
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Chlorpheniramine Maleate (UNII: V1Q0O9OJ9Z) (Chlorpheniramine - UNII:3U6IO1965U) Chlorpheniramine Maleate 1 mg  in 5 mL
    Pseudoephedrine hydrochloride (UNII: 6V9V2RYJ8N) (Pseudoephedrine - UNII:7CUC9DDI9F) Pseudoephedrine hydrochloride 15 mg  in 5 mL
    Dextromethorphan hydrobromide (UNII: 9D2RTI9KYH) (Dextromethorphan - UNII:7355X3ROTS) Dextromethorphan hydrobromide 5 mg  in 5 mL
    Inactive Ingredients
    Ingredient Name Strength
    anhydrous citric acid (UNII: XF417D3PSL)  
    FD&C red no. 40 (UNII: WZB9127XOA)  
    glycerin (UNII: PDC6A3C0OX)  
    propylene glycol (UNII: 6DC9Q167V3)  
    sodium benzoate (UNII: OJ245FE5EU)  
    sodium citrate, unspecified form (UNII: 1Q73Q2JULR)  
    sorbitol (UNII: 506T60A25R)  
    water (UNII: 059QF0KO0R)  
    Product Characteristics
    Color      Score     
    Shape Size
    Flavor CHERRY (wild cherry flavor) Imprint Code
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0904-5050-20 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/05/1997
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part341 01/05/1997
    Labeler - Major Pharmaceuticals, Inc (191427277)
    Registrant - Silarx Pharmaceuticals, Inc (161630033)
    Name Address ID/FEI Business Operations
    Bio-Pharm, Inc. 801652546 MANUFACTURE(0904-5050) , ANALYSIS(0904-5050) , PACK(0904-5050) , LABEL(0904-5050)