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Q Tapp Cold and Cough (Qualitest Pharmaceuticals)

Available Formats

Dosage Form Package Information Links
LIQUID 1 BOTTLE, PLASTIC in 1 CARTON (0603-0852-54) > 118 mL in 1 BOTTLE, PLASTIC Label Information
LIQUID 118 mL in 1 BOTTLE, PLASTIC (0603-0852-94) Label Information

Complete Q Tapp Cold and Cough Information

  • Active ingredients (in each 5 mL = 1 tsp)

    Brompheniramine maleate, USP 1 mg

    Dextromethorphan HBr, USP 5 mg

    Pseudoephedrine HCI, USP 15 mg


  • Purpose

    Antihistamine

    Cough suppressant

    Nasal decongestant


  • Uses

    • temporarily relieves cough due to minor throat and bronchial irritation occurring with a cold, and nasal congestion due to the common cold, hay fever or other upper respiratory allergies
    • temporarily relieves these symptoms due to hay fever (allergic rhinitis):
      • runny nose
      • sneezing
      • itchy, watery eyes
      • itching of the nose or throat
    • temporarily restores freer breathing through the nose

  • Warnings


  • Do not use

    • to sedate a child or to make a child sleepy
    • 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.

  • Ask a doctor before use if you have

    • heart disease
    • high blood pressure
    • thyroid disease
    • diabetes
    • trouble urinating due to an enlarged prostate gland
    • glaucoma
    • cough that occurs with too much phlegm (mucus)
    • a breathing problem or persistent or chronic cough that lasts such as occurs with smoking, asthma, chronic bronchitis, or emphysema

  • Ask a doctor or pharmacist before use if you are

    • taking any other oral nasal decongestant or stimulant
    • taking sedatives or tranquilizers

  • When using this product

    • do not use more than directed
    • marked drowsiness may occur
    • avoid alcoholic beverages
    • alcohol, sedatives, and tranquilizers may increase drowsiness
    • be careful when driving a motor vehicle or operating machinery
    • excitability may occur, especially in children

  • Stop use and ask a doctor if

    • you get nervous, dizzy, or sleepless
    • symptoms do not get better within 7 days or are accompanied by fever
    • cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache

    These could be signs of a serious condition.


  • PREGNANCY OR BREAST FEEDING

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


  • Keep out of reach of children.

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


  • Directions

    • use an accurate measuring device to administer this medication 
    • do not take more than 4 doses in any 24-hour period

     adults and children
     12 years and over

     4 tsp every
     4 hours 

     children 6 years to
     under 12 years

     2 tsp every
     4 hours

     children under 6 years

     do not use


  • Other information

    • each tsp contains: sodium 2 mg
    • store at 15°- 30°C (59°- 86°F)

    You may report serious side effects to: 130 Vintage Drive, Huntsville, AL 35811.


  • Inactive ingredients

    citric acid, FD&C blue #1, FD&C red #40, flavors, glycerin, high fructose corn syrup, propylene glycol, purified water, saccharin sodium, sodium benzoate, sorbitol solution


  • SPL UNCLASSIFIED SECTION

    Made in the USA
    for Qualitest Pharmaceuticals
    Huntsville, AL 35811

    Rev. 1/15 R4
    8073581  0852


  • PRINCIPAL DISPLAY PANEL

    Label for Q-Tapp Cold & Cough Red Grape flavor

  • INGREDIENTS AND APPEARANCE
    Q TAPP COLD AND COUGH 
    brompheniramine maleate and dextromethorphan hbr and pseudoephedrine hcl liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0603-0852
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BROMPHENIRAMINE MALEATE (UNII: IXA7C9ZN03) (BROMPHENIRAMINE - UNII:H57G17P2FN) BROMPHENIRAMINE MALEATE 1 mg  in 5 mL
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 5 mg  in 5 mL
    PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F) PSEUDOEPHEDRINE HYDROCHLORIDE 15 mg  in 5 mL
    Inactive Ingredients
    Ingredient Name Strength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SORBITOL (UNII: 506T60A25R)  
    Product Characteristics
    Color RED (clear and dark red) Score     
    Shape Size
    Flavor GRAPE (red grape) Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0603-0852-54 1 in 1 CARTON 04/02/2002 01/31/2018
    1 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2 NDC:0603-0852-94 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/02/2002 01/31/2018
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH FINAL part341 04/02/2002 01/31/2018
    Labeler - Qualitest Pharmaceuticals (011103059)
    Establishment
    Name Address ID/FEI Business Operations
    Vintage Pharmaceuticals-Huntsville 825839835 MANUFACTURE(0603-0852)