Label: DAY-TIME COLD/FLU RELIEF- acetaminophen, dextromethorphan hydrobromide, phenylephrine hcl liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 29, 2023

If you are a consumer or patient please visit this version.

  • Drug FactsActive Ingredients (in each 15 mL, 1 tablespoon)

    Acetaminophen 325 mg

    Dextromethorphan HBr 10 mg

    Phenylephrine HCL 5 mg

  • Purpose

    Pain reliever/fever reducer

    Cough suppressant

    Nasal decongestant

  • Keep out of reach of children

    Keep this and all drugs out of the reach of children.

  • Uses

    temporaily relieves these common cold/flu symptoms:

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

    Warnings

    Liver warning: This product contains acetaminophen. Severe liver damage
    may occur if adult/child takes: ● 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 everyday while using this product.
    Allery Alert: Acetaminophen may cause severe skin reactions.
    Symptoms may include: ● skin reddening ● blisters ● rash
    If skin reaction occurs, stop use and seek medical help right away.
    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

    • if you are now taking a prescription monamine 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.
    • with any other drug containing acetaminophen (prescription or nonprescription) If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist
  • 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
    • persistant or chronic cough such as occur with smoking, asthma, or emphysema
    • cough accompanied by excessive phlegm (mucuc)
  • Ask a doctor or pharmacist before use if

    the user is taking the blood thinner warfarin

  • When using this product

    • do not use more than directed (see overdose warning)
    • avoid alcoholic drinks
  • Stop use and ask a doctor if

    • you get nervous, dizzy or sleepless
    • new symptoms occur
    • fever gets worse or lasts more than 3 days
    • pain or cough gets worse or lasts more than 5 days (children) 7 days (adults)
    • redness or swelling is present
    • 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.

  • Overdose warning:

    Taking more than the recommended dose (overdose) could cause serious health problems, including liver damage.  In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately. 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 recommended (see overdose warning)
    • use dosage cup or tablespoon (TBSP)
    • do not exceed 4 doses per 24 hours
     age dose
     adults and children 12 years and over 30 mL (2 TBSP) every 4 hours
     children 6 years to under 12 years 15 mL (1 TBSP) every 4 hours
     children 4 years to under 6 years ask a doctor
     children under 4 years do not use

    * When using Day Time and Night Time products, carefully read each label to ensure correct dosing.

  • Other information

    • sodium content per tablespoon: 10 mg
    • store at room temperature
  • OTHER SAFETY INFORMATION

    DO NOT USE IF IMPRINTED SHRINK BRAND IS MISSING OR BROKEN
    Failure to follow these warnings could result in serious consequences.

  • Inactive ingredients

    citric acid, FD and C Yellow # 6, flavor, glycerin, propylene glycol, prified water, saccharin sodium, sodium benzoate, sucrose

  • Questions?

    Call weekdays 1-877-798-5944

  • Product Label: DISCOUNT drug mart FOOD FAIR Orange Day-Time COLD/FLU RELIEF

    DTime 506

    *COMPARE TO THE ACTIVE INGREDIENTS IN VICKS® DAYQUIL®

    DISCOUNT

    drug mart

    FOOD FAIR

    Orange Day-Time Cold/Flu Relief

    Acetaminophen ...... Pain Reliever/Fever Reducer

    Dextromethorphan HBR ....... Cough Suppressant

    Phenylephrine HCL ....... Nasal Decongestant

    12 FL OZ (354 mL)

    * This product is not manufactured or distributed by Proctor and Gamble owner of the registered trademark Vicks® DayQuil®

    LR-064   REV 02

    SATISFACTION GUARANTEED

    IF DISSATISFIED, RETURN UNUSED PORTION AND PACKAGE TO THE STORE WHERE PURCHASED. IF UNABLE TO RETURN TO THE STORE, SEND REASON FOR DISSATISFACTION , NAME, ADDRESS AND EMPTY PACKAGE TO: DISCOUNT DRUG MART, 211 COMMERCE DRIVE MEDINNA, OHIO 44256

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  • INGREDIENTS AND APPEARANCE
    DAY-TIME COLD/FLU RELIEF 
    acetaminophen, dextromethorphan hydrobromide, phenylephrine hcl liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53943-506
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg  in 15 mL
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg  in 15 mL
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE5 mg  in 15 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorORANGE (ORANGE) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53943-506-28354 mL in 1 BOTTLE; Type 0: Not a Combination Product10/25/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01210/25/2014
    Labeler - Discount Drug Mart (047741335)