ZODRYL AC 35 (CHLORPHENIRAMINE MALEATE AND CODEINE PHOSPHATE) SUSPENSION [CODADOSE, INC.]

ZODRYL AC 35 (CHLORPHENIRAMINE MALEATE AND CODEINE PHOSPHATE) SUSPENSION [CODADOSE, INC.]
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NDC 43378-102-04
Set ID 07af42d8-4b0c-4cd1-b299-42dc12980b94
Category HUMAN OTC DRUG LABEL
Packager CodaDose, Inc.
Generic Name
Product Class
Product Number
Application Number PART341
  • OTC - ACTIVE INGREDIENT

    Chlorpheniramine maleate 0.250 mg/1mL: antihistamine; Codeine phosphate 1 mg/1mL: cough suppressant

  • PURPOSE

    Temporarily relieves: cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants; the intensity of coughing; the impulse to cough to help you go to sleep; temporarily decreases runny nose and reduces sneezing, itching of the nose or throat, and itchy, watery eyes due to hay fever or other upper respiratory allergies

    Warnings

  • OTC - DO NOT USE

    in children who have chronic pulmonary disease, shortness of breath, or who are taking other drugs unless directed by a doctor; for persistent or chronic cough such as occurs with asthma or if cough is accompanied by excessive phlegm (mucus) unless directed by a doctor

  • OTC - ASK DOCTOR

    before use if you or your child has glaucoma; a breathing problem such as emphysema or chronic bronchitis

  • OTC - ASK DOCTOR/PHARMACIST SECTION

    if you or your child are taking sedatives or tranquilizers

  • OTC - WHEN USING THIS PRODUCT

    do not exceed recommended dosage; may cause or aggravate constipation; may cause excitability in children; may cause drowsiness; alcohol, sedatives, and tranquilizers may increase the drowsiness effect

  • OTC - STOP USE AND ASK A DOCTOR IF

    cough persists for more than 1 week, tends to recur, or is accompanied by a fever, rash, or persistent headache.  These could be signs of a serious condition.

  • OTC - KEEP THESE AND ALL DRUGS OUT OF REACH OF CHILDREN

    In case of overdose, seek professional assistance for contact a Poison Control Center immediately.

    Directions:

    • Take every 4-6 hours

    • Use only with enclosed calibrated oral dispenser

    • Do not take more than 4 doses in 24 hours or as directed by a doctor

    Children 2 to under 6 years of age:  ask a doctor

    Other information store at controlled room temperature 20°-25°C (68°-77°F).

    INACTIVE INGREDIENT

    Citric acid, FD&C red #40, galloquinate, glycerin, grape flavor, magnesium aluminometasilicate, methylparaben, purified water, sodium citrate dihydrate, sucralose, xanthan gum

  • OTC – QUESTIONS SECTION

    Call 1-866-574-8861 24 hours a day, 7 days a week.

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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    Figure 1.  Primary Label- Front Page

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    Figure 2. Primary Label – Second Page

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    Figure 3. Primary Label – Last Page

  • INGREDIENTS AND APPEARANCE
    ZODRYL AC 35 
    chlorpheniramine maleate and codeine phosphate suspension
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43378-102
    Route of AdministrationORALDEA ScheduleCV    
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE1 mg  in 4 mL
    CODEINE PHOSPHATE (UNII: GSL05Y1MN6) (CODEINE - UNII:Q830PW7520) CODEINE PHOSPHATE4 mg  in 4 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    TANNIC ACID (UNII: 28F9E0DJY6)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    ColorredScore    
    ShapeSize
    FlavorGRAPEImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43378-102-04118 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34101/01/2040
    Labeler - CodaDose, Inc. (831355115)
    Registrant - Gorbec Pharmaceutical Services Inc. (791919678)
    Establishment
    NameAddressID/FEIBusiness Operations
    Gorbec Pharmaceutical Services Inc.791919678manufacture