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DayTime Cold Multi-Symptom (WALGREEN CO.)

Available Formats

Dosage Form Package Information Links
CAPSULE, LIQUID FILLED 3 BLISTER PACK in 1 CARTON (0363-0560-07) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK Label Information
CAPSULE, LIQUID FILLED 2 BLISTER PACK in 1 CARTON (0363-0560-08) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK Label Information

Complete DayTime Cold Multi-Symptom Information

  • Active ingredients (in each gelcap)

    Acetaminophen 325 mg
    Dextromethorphan HBr 10 mg
    Phenylephrine HCl 5 mg


  • Purpose

    Pain reliever/fever reducer
    Cough suppressant
    Nasal decongestant


  • Uses

    • temporarily relieves these common cold/flu symptoms:
      • minor aches and pains
      • nasal congestion
      • headache
      • cough
      • sinus congestion and pressure
      • sore throat
    • helps clear nasal passages
    • promotes nasal and sinus drainage
    • temporarily reduces fever

  • Warnings

    Liver warning: This product contains acetaminophen. The maximum daily dose of this product is 10 gelcaps (3,250 mg acetaminophen) in 24 hours. Severe liver damage may occur if you take:

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

    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.
    • if you have ever had an allergic reaction to this product or any of its ingredients

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

    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
    • nervousness, dizziness, or sleeplessness occur
    • pain, nasal congestion, or cough gets worse or lasts more than 7 days
    • new symptoms occur
    • fever gets worse or lasts more than 3 days
    • redness or swelling is present
    • persistent cough lasts for more than one week, tends to recur, or is accompanied by fever, rash or persistent headache

    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 (1-800-222-1222) 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)
    • adults and children 12 years and over
      • take 2 gelcaps every 4 hours
      • do not take more than 10 gelcaps in 24 hours
      • swallow whole; do not crush, chew or dissolve
    • children under 12 years: ask a doctor

  • Other information

    • TAMPER EVIDENT: DO NOT USE IF OUTER PACKAGE IS OPENED OR BLISTER IS TORN OR BROKEN
    • store at 25ºC (77ºF); excursions permitted between 15º-30ºC (59º-86ºF)
    • see end flap for expiration date and lot number

  • Inactive ingredients

    croscarmellose sodium, crospovidone, D&C red #28, FD&C blue #1, FD&C red #40, gelatin, hydroxypropyl cellulose, hypromellose, iron oxide black, iron oxide red, iron oxide yellow, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, pregelatinized starch, propylene glycol, shellac glaze, silica gel, stearic acid, titanium dioxide


  • Questions or comments?

    1-800-426-9391


  • Principal Display Panel

    Well at
    Walgreens

    WALGREENS PHARMACIST RECOMMENDEDÇ‚

    NDC 0363-0560-07

    DAYTIME
    MULTI-SYMPTOM
    NON-DROWSY
    Cold
    Acetaminophen /
    Fever / Headache / Sore Throat
    Dextromethorphan HBr / Coughing
    Phenylephrine HCl / Nasal Congestion

    Pain reliever, fever reducer, cough suppressant &
    nasal decongestant
    Fast-release Quick Gelsâ„¢

    36
    GELCAPS
    (24+12 FREE)

    Actual Size

    Compare to Tylenol® Cold
    Multi-Symptom Daytime Rapid
    Release Gels active ingredientsÇ‚Ç‚

    PSEUDOEPHEDRINE FREE

    Ç‚Walgreens Pharmacist Survey Study, November 2012.

    Ç‚Ç‚This product is not manufactured or distributed by
    McNeil Consumer Healthcare, owner of the registered
    trademark Tylenol® Cold Multi-Symptom Daytime Rapid Release Gels.

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

    50844    REV1113B56007

    DISTRIBUTED BY: WALGREEN CO.
    200 WILMOT RD., DEERFIELD, IL 60015

    Walgreens
    100% SATISFACTION GUARANTEED

    walgreens.com  ©2014 Walgreen Co.

    Walgreens 44-560

    Walgreens 44-560


  • INGREDIENTS AND APPEARANCE
    COLD  DAYTIME, MULTI-SYMPTOM, NON-DROWSY
    acetaminophen, dextromethorphan hbr, phenylephrine hcl tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0560
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 10 mg
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 5 mg
    Inactive Ingredients
    Ingredient Name Strength
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    CROSPOVIDONE (UNII: 2S7830E561)  
    D&C RED NO. 28 (UNII: 767IP0Y5NH)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
    POVIDONE (UNII: FZ989GH94E)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Product Characteristics
    Color RED, PURPLE Score no score
    Shape OVAL Size 19mm
    Flavor Imprint Code L;0
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0363-0560-08 2 in 1 CARTON 03/29/2008 08/08/2018
    1 12 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2 NDC:0363-0560-07 3 in 1 CARTON 03/29/2008
    2 12 in 1 BLISTER PACK; 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 03/29/2008
    Labeler - Walgreen Company (008965063)
    Establishment
    Name Address ID/FEI Business Operations
    LNK International, Inc. 832867894 MANUFACTURE(0363-0560)
    Establishment
    Name Address ID/FEI Business Operations
    LNK International, Inc. 832867837 PACK(0363-0560)