Home > Drugs A-Z > Day Time Night Time Sinus Relief

Day Time Night Time Sinus Relief (Walgeens Company)

Available Formats

Dosage Form Package Information Links
KIT 1 KIT in 1 CARTON (0363-1019-03) * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK Label Information

Complete Day Time Night Time Sinus Relief Information

  • Active ingredient for DAYTIME (in each liquid cap)

    Acetaminophen 325 mg

    Phenylephrine HCl 5 mg


  • Active ingredient for NIGHTTIME (in each liquid cap)

    Acetaminophen 325 mg

    Doxylamine succinate 6.25 mg

    Phenylephrine HCl 5 mg


  • Purpose (DAYTIME ONLY)

    Pain reliever

    Nasal decongestant


  • Purpose (NIGHTTIME ONLY)

    Pain reliever

    Antihistamine

    Nasal decongestant


  • Uses (DAYTIME ONLY)

    • temporarily relieves nasal and sinus symptoms: 
    • sinus pain
    • headache
    • nasal and sinus congestion


  • Uses (NIGHTTIME ONLY)

    • temporarily relieves nasal and sinus symptoms:
    • headache 
    • sinus pain
    • nasal and sinus congestion
    • runny nose and sneezing


  • Warnings (DAYTIME ONLY)

    Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take:

    • more than 12 liquid caps in 24 hours, which is the maximum daily amount 
    • with other drugs containing acetaminophen
    • 3 or more alcohol drinks every day while using this product

    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.

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

    When using this product
    • do not exceed recommended dosage

    Stop use and ask doctor if
    • redness or swelling is present
    • nervousness, dizziness or sleeplessness occur
    • pain or nasal congestion gets worse or lasts more than 7 days
    • fever gets worse or lasts more than 3 days 
    • new symptoms occur 

    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.

    Overdose warning: Taking more than the recommended dose (overdose) may cause liver damage. 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.


  • Warnings (NIGHTTIME ONLY)

    Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take:

    • more than 12 liquid caps in 24 hours, which is the maximum daily amount 
    • with other drugs containing acetaminophen
    • 3 or more alcohol drinks every day while using this product

     

    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.

    Ask a doctor before use if you have
    • liver disease
    • heart disease
    • high blood pressure
    • thyroid disease
    • diabetes
    • glaucoma
    • trouble urinating due to an enlarged prostate gland 
    • a breathing problem such as emphysema or chronic bronchitis

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

    When using this product
    • do not exceed recommended dosage
    • excitability may occur, especially in children 
    • marked drowsiness may occur
    • alcohol, sedatives, and tranquilizers may increase drowsiness
    • avoid alcoholic drinks
    • be careful when driving a motor vehicle or operating machinery

    Stop use and ask doctor if
    • nervousness, dizziness or sleeplessness occur
    • pain or nasal congestion gets worse or lasts more than 7 days
    • fever gets worse or lasts more than 3 days
    • redness or swelling is present
    • new symptoms occur 

    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.

    Overdose warning: Taking more than the recommended dose (overdose) may cause liver damage. 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 (DAYTIME ONLY)

    • take only as recommended(see overdose warning)
    • adults and children 12 years and over:
    • take 2 liquid caps with water every 4 hours
    • do not take more than 12 liquid caps in 24 hours
    • children under 12 years: do not use this adult product in children under 12 years of age; this will provide more than the recommended dose (overdose) and may cause liver damage.

  • Directions (NIGHTTIME ONLY)

    • take only as recommended(see overdose warning)
    • adults and children 12 years and over:
    • take 2 liquid caps with water every 4 hours
    • do not take more than 12 liquid caps in 24 hours
    • children under 12 years: do not use this adult product in children under 12 years of age; this will provide more than the recommended dose (overdose) and may cause liver damage.

  • Other information

    • store at controlled room temperature 15°C to 30°C (59°F to 86°F)
    • see end flap for expiration date and lot number
    • for better identification, keep liquid caps in carton until used


  • Inactive ingredients (DAYTIME ONLY)

    edible white ink, FD&C yellow #6, gelatin, glycerin, polyethylene glycol, povidone, propylene glycol, purified water, sorbitol


  • Inactive ingredients (NIGHTTIME ONLY)

    edible white ink, FD&C blue #1, gelatin, glycerin, polyethylene glycol, povidone, propylene glycol, purified water, sorbitol 


  • Questions

    1-800-706-5575


  • Principal Display Panel

    Combo Pack

    SINUS RELIEF NONDROWSY DAYTIME

    Acetaminophen/Sinus Headache & Pain

    Phenylephrine HCl/Sinus Pressure & Congestion

    32 LIQUID CAPS

    SINUS RELIEF NIGHTTIME

    Acetaminophen/Sinus Headache & Pain/

    Doxylamine Succinate/Runny Nose

    Phenylephrine HCl/Sinus Pressure & Congestion

    16 LIQUID CAPS

    48 TOTAL LIQUID CAPS

    day-night-sinus-relief-ctn


  • INGREDIENTS AND APPEARANCE
    DAY TIME NIGHT TIME SINUS RELIEF 
    acetaminophen, doxylamine succinate, phenylephrine hcl kit
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-1019
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0363-1019-03 1 in 1 CARTON
    Quantity of Parts
    Part # Package Quantity Total Product Quantity
    Part 1 4 BLISTER PACK 32 
    Part 2 2 BLISTER PACK 16 
    Part 1 of 2
    DAY TIME SINUS RELIEF 
    acetaminophen, phenylephrine hcl capsule, liquid filled
    Product Information
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 5 mg
    Inactive Ingredients
    Ingredient Name Strength
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    GELATIN (UNII: 2G86QN327L)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
    POVIDONES (UNII: FZ989GH94E)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SORBITOL (UNII: 506T60A25R)  
    Product Characteristics
    Color ORANGE Score no score
    Shape OVAL Size 20mm
    Flavor Imprint Code 48A
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 8 in 1 BLISTER PACK
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part341 03/01/2013
    Part 2 of 2
    NIGHT TIME SINUS RELIEF 
    acetaminophen, doxylamine succinate, phenylephrine hcl, capsule, liquid filled
    Product Information
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg
    DOXYLAMINE SUCCINATE (UNII: V9BI9B5YI2) (DOXYLAMINE - UNII:95QB77JKPL) DOXYLAMINE SUCCINATE 6.25 mg
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 5 mg
    Inactive Ingredients
    Ingredient Name Strength
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    GELATIN (UNII: 2G86QN327L)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
    POVIDONES (UNII: FZ989GH94E)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SORBITOL (UNII: 506T60A25R)  
    Product Characteristics
    Color BLUE Score no score
    Shape OVAL Size 20mm
    Flavor Imprint Code 47A
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 8 in 1 BLISTER PACK
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part341 03/01/2013
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part341 03/01/2013
    Labeler - Walgeens Company (008965063)