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Day Time (Premier Value)

Available Formats

Dosage Form Package Information Links
LIQUID 296 mL in 1 BOTTLE, PLASTIC (68016-142-01) Label Information
LIQUID 296 mL in 1 BOTTLE, PLASTIC (68016-142-01) Label Information
LIQUID 177 mL in 1 BOTTLE, PLASTIC (68016-142-06) Label Information
LIQUID 177 mL in 1 BOTTLE, PLASTIC (68016-142-06) Label Information

Complete Day Time Information

  • Active Ingredients

    Acetaminophen 325 mg
    Dextromethorphan HBr 10 mg
    Phenylephrine HCI 5 mg


  • Purposes

    Acetaminophen..................................Pain reliever/fever reducer
    Dextromethorphan HBr.....................Cough suppressant
    Phenylephrine HCI............................Nasal decongestant


  • Uses

    temporarily relieves these common cold/flu symptoms:
    minor aches and pains headache sore throat fever
    nasal congestion cough due to minor throat and bronchial irritation


  • Warnings

    Liver warning: This product contains acetaminophen.
    Severe liver damage may occur if you take:
    more than 6 doses (12 tablespoonfuls or 180 mL) in 24 hours for adults
    more than 5 doses (5 tablespoonfuls or 75 mL) in 24 hours for
    children 6-12 years old
    with other drugs containing acetaminophen
    3 or more alcoholic drinks everyday while using this product
    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

    if you are on a sodium-restricted diet
    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 two 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. with any other drug containing acetaminophen (prescription or
    non-prescription). If you are not sure whether a drug contains acetaminophen, ask a
    doctor or pharmacist.


  • Ask a doctor before use if you have

    liver disease heart disease thyroid disease diabetes high blood pressure
    persistent or chronic cough such as occurs with smoking, asthma or emphysema
    cough accompanied by excessive phlegm (mucus)
    trouble urinating due to enlarged prostate gland


  • Ask a doctor or pharmacist before use if the user is

    taking the blood thinning drug warfarin


  • When using this product

    avoid alcoholic drinks
    do not use more than directed (see overdose warning)


  • Stop use and ask a doctor if

    redness or swelling is present new symptoms occur
    you get nervous, dizzy or sleepless
    pain or cough gets worse or lasts more than 5 days (children) or 7 days (adults)
    fever gets worse or lasts more than 3 days
    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 this and all drugs out of the reach of children.

    Overdose Warning: Taking more than the recommended dose (overdose) could cause
    serious health problems, including liver damage. In case of accidental overdose, seek
    professional assistance or contact a Poison Control Center immediately. Quick medical
    attention is critical for adults as well as for children even if you do not notice any signs
    or symptoms.


  • Directions

    take only as recommended (see overdose warning)
    use dosage cup or tablespoon (TBSP)
    do not exceed 5 doses (children) or 6 doses (adults) per 24 hours
    Age Dose
    adults and children 12 years and older.........2 tablespoons (30 mL) every 4 hours
    children 6 years to under 12 years................ 1 tablespoon (15 mL) every 4 hours
    children 4 years to under 6 years...................do not use unless directed by a doctor
    children under 4 years.....................................do not use
    When using DayTime and NightTime products, carefully read each
    label to ensure correct dosing.


  • Other Information

    sodium content per tablespoon: 71 mg
    store at controlled room temperature


  • Inactive Ingredients

    citric acid, flavor, glycerin, polyethylene glycol,
    propylene glycol, purified water, saccharin sodium, sodium citrate,
    sucrose, yellow 6


  • Principal Display Panel

    Premier Value
    Day-time
    non-drowsy cold/flu relief
    compare to the active ingredients in Vicks Dayquil
    Acetaminophen Pain Reliever/fever reducer
    Dextromethorphan HBr Cough Suppressant
    Phenyleprhine HCI nasal decongestant
    10 fl oz (296mL)


  • Package Label

     Acetaminophen 325 mg, Dextromethorphan HBr 10 mg, Phenylephrine 5 mg

    Premier Value DayTime


  • INGREDIENTS AND APPEARANCE
    DAY TIME  WITH PE
    acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:68016-142
    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
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SACCHARIN SODIUM ANHYDROUS (UNII: I4807BK602)  
    TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
    SUCROSE (UNII: C151H8M554)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    Product Characteristics
    Color      Score     
    Shape Size
    Flavor ORANGE (Vicks Dayquil Type Flavor) Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:68016-142-01 296 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH FINAL part341 04/16/2009
    Labeler - Chain Drug Consortium, LLC (101668460)