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Panatuss PED (Seyer Pharmatec, Inc.)

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LIQUID 1 BOTTLE in 1 CARTON (11026-2775-4) > 118 mL in 1 BOTTLE Label Information

Complete Panatuss PED Information

  • ACTIVE INGREDIENT

    Active Ingredients                         Purpose
    (in each 5 mL teaspoonful)

    Chlophedianol HCl 25 mg ...................... Cough Suppressant

    Dexchlorpheniramine Maleate 2 mg ......... Antihistamine

    Pseudoephedrine HCl 60 mg ................... Nasal Decongestant


  • PURPOSE

    Purpose

    Cough Suppressant

    Antihistamine

    Nasal Decongestant


  • INDICATIONS & USAGE

    Uses

    Temporarily calms cough due to minor throat and bronchial irritation as may occur with the common cold

    • calms the cough control center and relieves coughing
    • non narcotic cough suppressant for the temporary relief of cough
    • temporarily relieves runny nose and alleviates sneezing, itching of the nose or throat and itchy, watery eyes due to hay fever or other upper respiratory allergies
    • temporarily relieves nasal congestion due to the common cold
    • helps decongest sinus openings and passages; temporarily relieves sinus congestion and pressure

  • WARNINGS

    Warnings

    When using this product

    • use only as directed by physician
    • may cause excitability especially in children
    • may cause marked drowsiness; alcohol, sedatives and tranquilizers may increase the drowsiness effect
    • avoid alcoholic beverages while taking this product
    • use caution when driving a motor vehicle or operating machinery

  • DO NOT USE


    Do not use

    • if you are now 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 prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product
    • if you have a breathing problem such as emphysema or chronic bronchitis, or if you have glaucoma or difficulty in urination due to enlargement of the prostate gland unless directed by a doctor
    • if you are taking sedatives or tranquilizers, without first consulting your doctor
    Stop use and ask a doctor if
    • nervousness, dizziness or sleeplessness occur
    • condition lasts for more than 7 days, comes back, or is accompanied by fever, rash or persistent headache. These could be signs of serious condition

  • KEEP OUT OF REACH OF CHILDREN

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


  • PREGNANCY OR BREAST FEEDING

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


  • DOSAGE & ADMINISTRATION

    Directions

    • take every 6 hours, not to exceed 4 doses in 24 hours or as directed by a physician

    Adults and Children 12 years of age and older
    1 teaspoonful (5 mL)
    Children 6 to under 12 years of age
    1/2 teaspoonful (2.5 mL)
    Children under 6 years of age
    Ask a doctor

  • INACTIVE INGREDIENT

    Inactive ingredients

    Citric acid, flavor, methylparaben, potassium citrate, potassium sorbate, propylparaben, propylene glycol, purified water, sorbitol, sucralose, xanthan gum


  • QUESTIONS

    Questions or comments?1-888-782-3585


  • INGREDIENTS AND APPEARANCE
    PANATUSS PED 
    chlophedianol hydrchloride, dexchlorpheniramine maleate, pseudoephedrine hydrochloride liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:11026-2775
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CHLOPHEDIANOL HYDROCHLORIDE (UNII: 69QQ58998Y) (CHLOPHEDIANOL - UNII:42C50P12AP) CHLOPHEDIANOL HYDROCHLORIDE 25 mg  in 5 mL
    DEXCHLORPHENIRAMINE MALEATE (UNII: B10YD955QW) (DEXCHLORPHENIRAMINE - UNII:3Q9Q0B929N) DEXCHLORPHENIRAMINE MALEATE 2 mg  in 5 mL
    PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F) PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg  in 5 mL
    Inactive Ingredients
    Ingredient Name Strength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    POTASSIUM CITRATE (UNII: EE90ONI6FF)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SORBITOL (UNII: 506T60A25R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    Color      Score     
    Shape Size
    Flavor FRUIT (Tropical Fruit) Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:11026-2775-4 1 in 1 CARTON
    1 118 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part341 12/15/2012
    Labeler - Seyer Pharmatec, Inc. (832947126)