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Daytime Cold and Flu Relief (Walgreen Company)

Available Formats

Dosage Form Package Information Links
LIQUID 177 mL in 1 BOTTLE (0363-0656-30) Label Information
LIQUID 296 mL in 1 BOTTLE (0363-0656-38) Label Information
LIQUID 237 mL in 1 BOTTLE (0363-0656-34) Label Information
LIQUID 355 mL in 1 BOTTLE (0363-0656-40) Label Information

Complete Daytime Cold and Flu Relief Information

  • Active ingredients (in each 15 ml tablespoon)

    Acetaminophen 325 mg

    Dextromethorphan HBr 10 mg

    Phenylephrine HCl 5 mg


  • Purpose

    Pain reliever/fever reducer

    Cough suppressant

    Nasal decongestant


  • Uses

    temporarily relieves common cold/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. The maximum daily dose of this product is 4 doses (adult: 2,600 mg acetaminophen; child: 1,300 mg acetaminophen) in 24 hours. Severe liver damage may occur if

    • adult takes more than 4,000 mg of acetaminophen in 24 hours
    • child takes more than 5 doses in 24 hours, which is the maximum daily amount
    • taken with other drugs containing acetaminophen
    • adult has 3 or more alcoholic drinks every day while using this product

    Sore throat warning: If sore throat is severe, lasts for more than 2 days, occurs with or is 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
    • heart disease
    • thyroid disease
    • diabetes
    • high blood pressure
    • trouble urinating due to an enlarged prostate gland
    • cough that occurs with too much phlegm (mucus)
    • persistent or chronic cough as occurs with smoking, asthma, or emphysema

    Ask a doctor or pharmacist before use if you are

    taking the blood thinning drug warfarin

    When using this product

    do not use more than directed

    Stop use and ask a doctor if
    • you get nervous, dizzy or sleepless
    • pain, nasal congestion or cough gets worse or lasts more than 5 days (children) or 7 days (adults)
    • fever gets worse or lasts more than 3 days
    • redness or swelling is present
    • new symptoms occur
    • 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 out of reach of children.

    In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222) 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 Liver warning
    • use dose cup
    • do not exceed 4 doses per 24 hrs

    adults & children 12 yrs & over

    30 ml (2 TBSP) every 4 hrs

    children 6 to under 12 yrs

    15 ml (1 TBSP) every 4 hrs

    children 4 to under 6 yrs

    ask a doctor

    children under 4 yrs

    do not use

    • when using other Daytime or Nighttime products, carefully read each label to insure correct dosing

  • Other information

    • each tablespoon contains: sodium 7 mg
    • store at 20°-25°C (68°-77°F)

  • Inactive ingredients

    butylated hydroxyanisole, edetate disodium, FD&C yellow no. 6, flavor, glycerin, menthol, monobasic sodium phosphate, polyethylene glycol, propylene glycol, purified water, saccharin sodium, sucrose, xanthan gum


  • Questions or comments?

    1-800-719-9260


  • Principal Display Panel

    NON-DROWSY - DAYTIME

    Cold & Flu Relief

    Acetaminophen / Aches / Fever

    Dextromethorphan HBr / Cough

    Phenylephrine HCl / Nasal Congestion

    Pain reliever, fever reducer, cough suppressant & nasal decongestant

    Alcohol free

    Antihistamine free

    Compare to Vicks® DayQuil® active ingredients

    Cold & Flu Relief Label Image 1
    Cold & Flu Relief Label Image 2

  • INGREDIENTS AND APPEARANCE
    DAYTIME COLD AND FLU RELIEF  NON DROWSY
    acetaminophen, dextromethorphan hbr, phenylephrine hcl liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0656
    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
    BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    MENTHOL (UNII: L7T10EIP3A)  
    SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)  
    POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SUCROSE (UNII: C151H8M554)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    Color ORANGE (clear) Score     
    Shape Size
    Flavor MENTHOL (with fruit) Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0363-0656-30 177 mL in 1 BOTTLE
    2 NDC:0363-0656-38 296 mL in 1 BOTTLE
    3 NDC:0363-0656-40 355 mL in 1 BOTTLE
    4 NDC:0363-0656-34 237 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part341 07/07/2006
    Labeler - Walgreen Company (008965063)