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Daytime Sinus (VALU MERCHANDISERS COMPANY)

Available Formats

Dosage Form Package Information Links
CAPSULE, LIQUID FILLED 1 BLISTER PACK in 1 BOX (63941-341-86) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK Label Information
CAPSULE, LIQUID FILLED 2 BLISTER PACK in 1 BOX (63941-341-51) > 20 CAPSULE, LIQUID FILLED in 1 BLISTER PACK Label Information

Complete Daytime Sinus Information

  • ACTIVE INGREDIENTS (IN EACH SOFTGEL)

    Acetaminophen 325mg

    Phenylephrine HCI 5mg


  • PURPOSES

    Pain Reliever

    Nasal decongestant


  • USES

    temporarily relieves common cold and flu symptoms:

    • nasal congestion
    • cough due to minor throat and bronchial irritation
    • sore throat
    • headache
    • minor aches and pains, fever

  • WARNINGS

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

    • more than 4 doses in 24 hours, which is the maximum daily amount for this product
    • with other drugs containing acetaminophen
    • 3 or more alcoholic drinks every day while using this product.

    Do Not Use
    • with any other products 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 Disease), or for 2 weeks after stopping the MAOI drugs. 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
    • thyroid disease
    • diabetes
    • high blood pressure
    • trouble urinating due to enlarged prostate gland

    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 a doctor if
    • you get nervous, dizzy or sleepless
    • symptoms get worse or last more than 7 days or are accompanied by a fever
    • fever gets worse or lasts more than 3 days
    • redness or swelling is present
    • new symptoms occur

    If pregnant or breast-feeding,

    ask a health professional before use

    Keep out of reach of children

    In case of accidental overdose, contact a doctor or Poison Control Center immediately (1-800-222-1222). Taking more than the recommended dose (overdose) may cause liver damage. 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 directed (see Warnings)
    • do not exceed 4 doses per 24 hours
      Adults and children 12 years and over take 2 softgels with water every 4 hours
      Children 4 to under 12 years Ask a doctor
      Children under 4 years Do not use

  • OTHER INFORMATION

    • store at room temperature
    • do not use if blister is torn or open

  • INACTIVE INGREDIENTS

    FD&C Yellow #6, gelatin, glycerin, polyethylene glycol 400, povidone, propylene glycol, purified water, sorbitol sorbitan, titanium dioxide.


  • QUESTIONS OR COMMENTS?

    Call toll free 1-888-952-0050 Monday through Friday 9AM-5PM EST


  • PRINCIPAL DISPLAY PANEL

    Multi-Symptom ∙ Sinus Relief

    Now Drowsy

    Acetaminophen/Phenylephrine HCI

    Pain reliever/Fever Reducer/Nasal Decongestant

    Alcohol free/Antihistamine Free

    Keep outer carton for complete warnings and product information

    Proudly Distributed by:

    Valu Merchandisers, Co.

    Kansas City, KS 66106

    This product is packaged in a child resistant and tamper evidence package.

    Use only if blisters are intact.

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

    BCDaytimeSinus12ct

    BCDaytimeSinus20ct

  • INGREDIENTS AND APPEARANCE
    DAYTIME SINUS  
    acetaminophen and phenylephrine hci capsule, liquid filled
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:63941-341
    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)  
    WATER (UNII: 059QF0KO0R)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    SORBITOL (UNII: 506T60A25R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    POVIDONE (UNII: FZ989GH94E)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    Product Characteristics
    Color orange Score no score
    Shape CAPSULE Size 23mm
    Flavor Imprint Code 224
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:63941-341-86 1 in 1 BOX
    1 12 in 1 BLISTER PACK
    2 NDC:63941-341-51 2 in 1 BOX
    2 20 in 1 BLISTER PACK
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part341 05/29/2012
    Labeler - VALU MERCHANDISERS COMPANY (868703513)
    Registrant - A&Z Pharmaceutical, Inc. (926820705)
    Establishment
    Name Address ID/FEI Business Operations
    A&Z Pharmaceutical, Inc. 926820705 manufacture(63941-341) , pack(63941-341)