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DayTime Nitetime Sinus Relief (TOP CARE (Topco Associates LLC))

Available Formats

Dosage Form Package Information Links
KIT 1 KIT in 1 CARTON (36800-102-48) * 8 CAPSULE in 1 BLISTER PACK * 8 CAPSULE in 1 BLISTER PACK Label Information

Complete DayTime Nitetime Sinus Relief Information

  • Active ingredients in Daytime (in each softgel)

    Acetaminophen 325 mg

    Phenylephrine HCl 5 mg


  • Active ingredients in Nighttime (in each softgel)

    Acetaminophen 325 mg

    Doxylamine succinate 6.25 mg

    Phenylephrine HCl 5 mg


  • Purpose for Daytime

    Pain reliever

    Nasal decongestant


  • Purpose for Nighttime

    Pain reliever

    Antihistamine

    Nasal decongestant


  • Uses

    • temporarily relieves nasal and sinus symptoms:
      • sinus pain
      • headache
      • nasal and sinus congestion
      • runny nose and sneezing (Nighttime only)

  • Warnings

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

    • more than 4,000 mg of acetaminophen in 24 hours 
    • with other drugs containing acetaminophen
    • 3 or more alcoholic drinks every day while using this product

    Do not use
    • to make a child sleep (Nighttime only)
    • 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
    • diabetes
    • high blood pressure
    • thyroid disease
    • trouble urinating due to an enlarged prostate gland
    • a breathing problem such as emphysema or chronic bronchitis (Nighttime only)
    • glaucoma (Nighttime only)

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

    When using this product,

    do not exceed recommended dosage. In addition, when using Nighttime:

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

    Stop use and ask a 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 can 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

    • do not take more than directed (see Overdose warning) 
    • do not take more than 4 doses in 24 hours
    • swallow whole; do not crush, chew, or dissolve

    Daytime: adults and children 12 years and over: take 2 softgels with water every 4 hours.

    Nighttime: adults and children 12 years and over: take 2 softgels with water every 4 hours.

    • children under 12 years: do not use

  • Other information

    • store at room temperature 15°-30°C (59°-86°F)
    • avoid excessive heat

  • Inactive ingredients in Daytime

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


  • Inactive ingredients in Nighttime

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


  • Questions or comments?

    Call toll free 1-888-423-0139


  • Principal Display Panel

    When using Daytime and Nighttime products, carefully read the labeling to insure correct dosing

    NON-DROWSY Daytime Sinus Relief

    PAIN RELIEVER AND NASAL DECONGESTANT

    • Aches: ACETAMINOPHEN, 325 mg
    • Nasal Congestion: Phenylephrine HCl, 5 mg

    †Supports Children's Miracle Network Hospitals Helping Local Kids

    DAYTIME SOFTGELS

    MULTI-SYMPTOM Nitetime Sinus Relief

    PAIN RELIEVER, ANTIHISTAMINE, AND NASAL DECONGESTANT

    • Aches: ACETAMINOPHEN, 325 mg
    • Sneezing/Runny Nose: Doxylamine succinate, 6.25 mg
    • Nasal Congestion: Phenylephrine HCl, 5 mg

    COMPARE TO VICKS® DAYQUIL® AND NYQUIL® SINEX® LIQUICAPS® active ingredients*

    NITETIME SOFTGELS

    *This product is not manufactured or distributed by Procter & Gamble, owner of the registered trademark Vicks® DayQuil® and NyQuil® Sinex® LiquiCaps®.

    †A portion of the proceeds from this purchase will support the Children's Miracle Network Hospitals.

    DISTRIBUTED BY TOPCO ASSOCIATES LLC

    ELK GROVE VILLAGE, IL  60007

    1-888-423-0139  topcare@topco.com

    Product of Canada

    TAMPER EVIDENT: DO NOT USE IF CARTON IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING.

    KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.


  • Product Label

    Acetaminophen 325 mg, Phenylephrine HCl 5 mg, Doxylamine succinate 6.25 mg, Phenylephrine HCl 5 mg

    Top Care Daytime and Nitetime Sinus Relief Softgels


  • INGREDIENTS AND APPEARANCE
    DAYTIME NITETIME SINUS RELIEF 
    acetaminophen, doxylamine succinate, phenylephrine hcl kit
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:36800-102
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36800-102-48 1 in 1 CARTON
    Quantity of Parts
    Part # Package Quantity Total Product Quantity
    Part 1 2 BLISTER PACK 16 
    Part 2 4 BLISTER PACK 32 
    Part 1 of 2
    NITETIME SINUS RELIEF 
    acetaminophen, doxylamine succinate, phenylephrine hcl capsule
    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)  
    SORBITAN (UNII: 6O92ICV9RU)  
    Product Characteristics
    Color BLUE Score no score
    Shape CAPSULE 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
    Part 2 of 2
    DAYTIME SINUS RELIEF 
    acetaminophen, phenylephrine hcl capsule
    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)  
    SORBITAN (UNII: 6O92ICV9RU)  
    Product Characteristics
    Color ORANGE Score no score
    Shape CAPSULE 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 01/15/2013
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH FINAL part341 01/15/2013
    Labeler - TOP CARE (Topco Associates LLC) (006935977)