DAYTIME COUGH NIGHTTIME COUGH (DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE) KIT [CVS PHARMACY]

DAYTIME COUGH NIGHTTIME COUGH (DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE) KIT [CVS PHARMACY]
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NDC 59779-031-02, 59779-668-40
Set ID 4d6df7fa-33ed-4715-98fb-f35bd424b30a
Category HUMAN OTC DRUG LABEL
Packager CVS Pharmacy
Generic Name
Product Class Antihistamine
Product Number
Application Number PART341
  • Active ingredients (in each 30 mL) - Nighttime Cough

    Dextromethorphan HBr 30 mg

    Doxylamine succinate 12.5 mg

  • Purpose - Nighttime Cough

    Cough suppressant

    Antihistamine

  • Uses – Nighttime Cough

    temporarily relieves cold symptoms:

    runny nose and sneezing
    cough due to minor throat and bronchial irritation
  • Warnings

  • Do not use – Nighttime Cough

    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 – Nighttime Cough

    glaucoma
    cough that occurs with too much phlegm (mucus)
    a breathing problem such as emphysema or chronic bronchitis
    persistent or chronic cough as occurs with smoking, asthma, or emphysema
    trouble urinating due to an enlarged prostate gland
  • Ask a doctor or pharmacist before use if you are – Nighttime Cough

    taking sedatives or tranquilizers

  • When using this product – Nighttime Cough

    excitability may occur, especially in children
    avoid alcoholic drinks
    may cause marked drowsiness
    be careful when driving a motor vehicle or operating machinery
    alcohol, sedatives, and tranquilizers may increase drowsiness
  • Stop use and ask a doctor if - Nighttime Cough

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

  • If pregnant or breast-feeding, - Nighttime Cough

    ask a health professional before use.

  • Keep out of reach of children. - Nighttime Cough

    In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

  • Directions – Nighttime Cough

    take only as directed
    only use the dose cup provided
    do not exceed 4 doses per 24 hrs

    adults & children 12 yrs & over

    30 mL every 6 hrs

    children 4 to under 12 yrs

    ask a doctor

    children under 4 yrs

    do not use

  • Other information – Nighttime Cough

    each 30 mL contains: sodium 32 mg
    store at 20-25°C (68-77°)
  • Inactive ingredients – Nighttime Cough

    alcohol, anhydrous citric acid, FD&C blue #1, FD&C red #40, flavor, high fructose corn syrup, polyethylene glycol, propylene glycol, purified water, saccharin sodium, sodium citrate

  • Questions or comments – Nighttime Cough

    1-800-719-9260

  • Active ingredient (in each 15 mL) - Daytime Cough

    Dextromethorphan HBr 15 mg

  • Purpose - Daytime Cough

    Cough suppressant

  • Uses – Daytime Cough

    temporarily relieves cough due to minor throat and bronchial irritation associated with a cold

  • Warnings

  • Do not use – Daytime Cough

    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 – Daytime Cough

    cough that occurs with too much phlegm (mucus)
    persistent or chronic cough as occurs with smoking, asthma, or emphysema
  • Stop use and ask a doctor if – Daytime Cough

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

  • If pregnant or breast-feeding, - Daytime Cough

    ask a health professional before use.

  • Keep out of reach of children. – Daytime Cough

    In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

  • Directions – Daytime Cough

    take only as directed
    only use the dose cup provided
    do not exceed 4 doses per 24 hrs

    adults & children 12 yrs & over

    30 mL every 6-8 hrs

    children 6 to under 12 yrs

    15 mL every 6-8 hrs

    children 4 to under 6 yrs

    ask a doctor

    children under 4 yrs

    do not use

  • Other information – Daytime Cough

    each 15 mL contains: sodium 13 mg
    store at 20-25°C (68-77°F)
    does not meet USP requirements for light resistant packaging
  • Inactive ingredients – Daytime Cough

    anhydrous citric acid, D&C yellow #10, FD&C yellow #6, flavor, high fructose corn syrup, polyethylene glycol, propylene glycol, purified water, saccharin sodium, sodium citrate

  • Questions or comments? – Daytime Cough

    1-800-719-9260

  • Principal Display Panel – Nighttime Cough

    DAY & NIGHT COMBO PACK

    Compare to the active ingredient in Vicks® DayQuil® Cough

    Cough Relief

    Non-Drowsy

    Daytime Cough

    DEXTROMETHORPHAN HBr

    Cough suppressant

    Powerful cough relief for up to 8 hours

    Antihistamine free

    Alcohol free

    Citrus Blend Flavor

    Compare to the active ingredients in Vicks® NyQuil® Cough

    Cough Relief

    Nighttime Cough

    DEXTROMETHORPHAN HBr

    Cough suppressant

    DOXYLAMINE SUCCINATE

    Antihistamine

    Relieves:

    Cough

    Sneezing

    Runny nose

    ALCOHOL 10%

    Cherry Flavor

    TWO 12 FL OZ (355 mL) UNITS TOTAL 24 FL OZ (1.5 PT) (710 mL)

    Daytime Cough Nighttime Cough Label Image 1
    Daytime Cough Nighttime Cough Label Image 2
  • INGREDIENTS AND APPEARANCE
    DAYTIME COUGH NIGHTTIME COUGH 
    dextromethorphan hbr, doxylamine succinate kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-031
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59779-031-021 in 1 CARTON; Type 0: Not a Combination Product08/07/2012
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 BOTTLE 355 mL
    Part 21 BOTTLE 355 mL
    Part 1 of 2
    NIGHTTIME COUGH 
    dextromethorphan hydrobromide, doxylamine succinate solution
    Product Information
    Item Code (Source)NDC:59779-668
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE30 mg  in 30 mL
    DOXYLAMINE SUCCINATE (UNII: V9BI9B5YI2) (DOXYLAMINE - UNII:95QB77JKPL) DOXYLAMINE SUCCINATE12.5 mg  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
    POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    Product Characteristics
    ColorRED (Dark Red) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59779-668-40355 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34109/23/2002
    Part 2 of 2
    DAYTIME COUGH 
    dextromethorphan hbr solution
    Product Information
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE15 mg  in 15 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
    POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    Product Characteristics
    ColorORANGE (light) Score    
    ShapeSize
    FlavorCITRUS (blend) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1355 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34108/07/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34108/07/2012
    Labeler - CVS Pharmacy (062312574)

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