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Daytime NiteTime (Kroger Company)

Available Formats

Dosage Form Package Information Links
KIT 1 KIT in 1 PACKAGE (30142-926-01) * 295 mL in 1 BOTTLE (30142-041-38) * 295 mL in 1 BOTTLE (30142-656-38) Label Information

Complete Daytime NiteTime Information

  • Active ingredient (in each 15 mL tablespoon) (for Nighttime)

    Acetaminophen 500 mg

    Dextromethorphan HBr 15 mg

    Doxylamine succinate 6.25 mg


  • Active ingredient (in each 15 mL tablespoon)  (for Daytime)

    Acetaminophen 325 mg

    Dextromethorphan HBr 10 mg

    Phenylephrine HCl 5 mg


  • Purpose (for Nighttime)

    Pain reliever/fever reducer

    Cough suppressant

    Antihistamine


  • Purpose (for Daytime)

    Pain reliever/fever reducer

    Cough suppressant

    Nasal decongestant


  • Uses

    temporarily relieves common cold/flu symptoms:

    • nasal congestion (Daytime only)
    • sore throat
    • cough due to minor throat and bronchial irritation
    • headache
    • minor aches and pains
    • fever
    • runny nose and sneezing (Nighttime only)

  • Warnings

    Liver warning: These products contain acetaminophen. Severe liver damage may occur if:

    • adult takes more than 4 doses in 24 hours (Nighttime) or more than 6 doses in 24 hours (Daytime), which is the maximum daily amount
    • child takes more than 5 doses in 24 hours (Daytime)
    • taken with other drugs containing acetaminophen
    • adult has 3 or more alcoholic drinks every day while using these products

    Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.

    Do not use
    • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
    • 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.
    • to make a child sleepy

    Ask a doctor before use if you have
    • high blood pressure (Daytime only)
    • heart disease (Daytime only)
    • diabetes (Daytime only)
    • thyroid disease (Daytime only)
    • trouble urinating due to an enlarged prostate gland
    • liver disease
    • cough that occurs with too much phlegm (mucus)
    • persistent or chronic cough as occurs with smoking, asthma or emphysema
    • a breathing problem such as emphysema or chronic bronchitis (Nighttime only)
    • glaucoma (Nighttime only)
    • a sodium-restricted diet (Nighttime only)

    Ask a doctor or pharmacist before use if you are
    • taking sedatives or tranquilizers
    • taking the blood thinning drug warfarin

    When using these products
    • do not use more than directed

    In addition, when using Nighttime:

    • avoid alcoholic drinks
    • marked drowsiness may occur
    • excitability may occur, especially in children
    • alcohol, sedatives and tranquilizers may increase drowsiness
    • be careful when driving a motor vehicle or operating machinery

    Stop use and ask a doctor if
    • you get nervous, dizzy or sleepless (Daytime only)
    • new symptoms occur
    • fever gets worse or lasts more than 3 days
    • redness or swelling is present
    • pain, nasal congestion or cough gets worse or lasts more than 5 days (children) or 7 days (adults)
    • cough comes back or occurs with rash or headache that lasts. These could be signs of a serious condition.

    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. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.


  • Directions

    • take as recommended - see Liver warning
    • take Nighttime OR Daytime
    • use dose cup

    Nighttime Liquid

    • do not exceed 4 doses per 24 hours
    adults and children 12 years and over 30 mL (2 TBSP) every 6 hours
    children 4 to under 12 years ask a doctor
    children under 4 years do not use

    Daytime Liquid

    • do not exceed 5 doses (children) or 6 doses (adults) per 24 hours
    adults and children 12 years and over 30 mL (2 TBSP) every 4 hours
    children 6 to under 12 years 15 mL (1 TBSP) every 4 hours
    children 4 to under 6 years ask a doctor
    children under 4 years do not use
    • when using other Daytime or Nighttime products, carefully read each label to insure correct dosing

  • Other information

    • each TBSP of Nighttime contains: sodium 18 mg
    • each TBSP of Daytime contains: sodium 7 mg
    • store at 20°-25°C (68°-77°F)

  • Inactive ingredients

    Nighttime

    alcohol, anhydrous citric acid, FD&C blue no. 1, FD&C red no. 40, flavor, high fructose corn syrup, polyethylene glycol, propylene glycol, purified water, saccharin sodium, sodium citrate

    Daytime

    butylated hydroxyanisole, edetate disodium, FD&C yellow no. 6, flavors, glycerin, monobasic sodium phosphate, polyethylene glycol, propylene glycol, purified water, saccharin sodium, sucrose, xanthan gum


  • Questions or comments?

    1-800-632-6900


  • Principal Display Panel

     Sealed with printed neckband for your protection. If missing or broken return to store.

    Save when you buy Day Time and Nite Time!

    (For Daytime)

    Compare to active ingredients of Vicks® DayQuil® - see bottom panel

    Alcohol Free/Antihistamine Free

    See New Warnings Information

    Multi-Symptom Cold/Flu Relief

    Non-Drowsy

    Day Time

    Pain Reliever/Fever Reducer - Acetaminophen

    Cough Suppressant - Dextromethorphan HBr

    Nasal Decongestant - Phenylephrine HCl

    Aches/Fever

    Cough

    Nasal Congestion

    Original Flavor

    (For Nighttime)

    Compare to active ingredients of Vicks® NyQuil® - see bottom panel

    Alcohol 10%

    See New Warnings Information

    Multi-Symptom Cold/Flu Relief

    Nite Time

    Pain Reliever/Fever Reducer - Acetaminophen

    Cough Suppressant - Dextromethorphan HBr

    Antihistamine - Doxylamine Succinate

    Aches/Fever

    Cough/Sneezing

    Runny Nose

    Cherry Flavor

    Day Time and Nite Time Cold/Flu Relief Combo Pack Carton Image 1

    Day Time and Nite Time Cold/Flu Relief Combo Pack Carton Image 1

    Day Time and Nite Time Cold/Flu Relief Combo Pack Carton Image 2

    Day Time and Nite Time Cold/Flu Relief Combo Pack Carton Image 2


  • INGREDIENTS AND APPEARANCE
    DAYTIME NITETIME 
    acetaminophen, dextromethorphan hbr, doxylamine succinate, phenylephrine hcl kit
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-926
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:30142-926-01 1 in 1 PACKAGE
    Quantity of Parts
    Part # Package Quantity Total Product Quantity
    Part 1 1 BOTTLE 296 mL
    Part 2 1 BOTTLE 296 mL
    Part 1 of 2
    NITE TIME COLD AND FLU RELIEF 
    acetaminophen, dextromethorphan hydrobromide and doxylamine succinate liquid
    Product Information
    Item Code (Source) NDC:30142-041
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 500 mg  in 15 mL
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 15 mg  in 15 mL
    DOXYLAMINE SUCCINATE (UNII: V9BI9B5YI2) (DOXYLAMINE - UNII:95QB77JKPL) DOXYLAMINE SUCCINATE 6.25 mg  in 15 mL
    Inactive Ingredients
    Ingredient Name Strength
    ALCOHOL (UNII: 3K9958V90M)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    WATER (UNII: 059QF0KO0R)  
    HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    Product Characteristics
    Color RED (Clear Dark) Score     
    Shape Size
    Flavor CHERRY Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:30142-041-38 295 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part341 05/21/2009
    Part 2 of 2
    DAY TIME  NON DROWSY MULTI SYMPTOM COLD FLU RELIEF
    acetaminophen, dextromethorphan hbr, phenylephrine hcl liquid
    Product Information
    Item Code (Source) NDC:30142-656
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg  in 15 mL
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 10 mg  in 15 mL
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 5 mg  in 15 mL
    Inactive Ingredients
    Ingredient Name Strength
    BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)  
    POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SUCROSE (UNII: C151H8M554)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    Color ORANGE (clear) Score     
    Shape Size
    Flavor MENTHOL (with fruit) Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:30142-656-38 295 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part341 06/11/2006
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part341 08/28/2006
    Labeler - Kroger Company (006999528)