NIGHTTIME COLD AND FLU (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE AND DOXYLAMINE SUCCINATE) LIQUID [BI-MART]

NIGHTTIME COLD AND FLU (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE AND DOXYLAMINE SUCCINATE) LIQUID [BI-MART]
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NDC 37835-952-30
Set ID 1eda2750-340e-4f80-a109-575111eab0a4
Generic Name
Product Class Antihistamine
Product Number
Application Number PART341
  • Drug Facts

    Active ingredients (in each 30 mL dose cup)

    Acetaminophen, USP 650 mg
    Dextromethorphan HBr, USP 30 mg
    Doxylamine succinate, USP 12.5 mg

  • Purpose

    Pain reliever/fever reducer
    Cough suppressant
    Antihistamine

  • Uses

    temporarily relieves common cold/flu symptoms:

    • cough due to minor throat and bronchial irritation
    • sore throat
    • headache
    • minor aches and pains
    • fever
    • runny nose and sneezing
  • Warnings

    Liver warning:


    This product contains 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

    Allergy alert:


    Acetaminophen may cause severe skin reactions. Symptoms may include:

    • skin reddening
    •  blisters
    •  rash.

    If a skin reaction occurs, stop use and seek medical help right away.


    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, see 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.
    • to make a child sleep.
  • Ask a doctor before use if you have


    • liver disease
    • glaucoma
    •  cough that occurs with too much phlegm (mucus)
    •  a breathing problem or chronic cough that lasts or as occurs with smoking, asthma, chronic bronchitis or emphysema
    • trouble urinating due to enlarged prostate gland
    • a sodium-restricted diet
  • Ask a doctor or pharmacist before use if you are


    • taking sedatives or tranquilizers
    •  taking the blood thinning drug warfarin
  • When using this product


    • do not use more than directed
    • 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


    • pain or cough 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
    •  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.

    Overdose warning:

    Taking more than the directed can cause serious health problems. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Prompt 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 Overdose warning
    •  use dose cup or tablespoon (TBSP)
    •  do not exceed 4 doses (120 mL) (8 TBSP) per 24 hours
    •  mL = milliliter; TBSP = tablespoon

    adults & children 12 years & over 
    30 mL (2 TBSP) every 6 hours 
    children 4 to under 12 years
    ask a doctor 
    children under 4 years
    do not use 

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

    • each 30 mL dose cup contains: potassium 5 mg, sodium 37 mg
    • store at 20° to 25°C (68° to 77°F)
  • Inactive ingredients

    acesulfame potassium, alcohol, anhydrous citric acid, D&C yellow no.10, FD&C green no. 3, FD&C yellow no. 6, flavors, high fructose corn syrup, polyethylene glycol, propylene glycol, purified water, saccharin sodium, sodium citrate

  • Questions or Comments?

    call 1-800-935-6737

    Distributed by:
    BI-MART
    Eugene, OR 97402

  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 12 FL OZ (355 mL Bottle)

    BI-MART

    Compare to the active ingredients
    in Vicks® NyQuil® Cold & Flu*

    NIGHTTIME
    COLD & FLU

    Acetaminophen USP (Pain reliever/fever reducer)
    Doxylamine succinate USP (Antihistamine)
    Dextromethorphan HBr USP (Cough suppressant)


    • Aches, Fever & Sore Throat
    • Sneezing, Runny Nose
    • Cough 

    Alcohol 10%

    12 FL OZ (355 mL)



    PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 12 FL OZ (355 mL Bottle)

  • INGREDIENTS AND APPEARANCE
    NIGHTTIME COLD AND FLU 
    acetaminophen, dextromethorphan hydrobromide and doxylamine succinate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37835-952
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN650 mg  in 30 mL
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE30 mg  in 30 mL
    DOXYLAMINE SUCCINATE (UNII: V9BI9B5YI2) (DOXYLAMINE - UNII:95QB77JKPL) DOXYLAMINE SUCCINATE12.5 mg  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)  
    ALCOHOL (UNII: 3K9958V90M)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    ANISE (UNII: 21C2F5E8RE)  
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
    HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    Product Characteristics
    ColorGREENScore    
    ShapeSize
    FlavorANISE, MENTHOLImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37835-952-30355 mL in 1 BOTTLE; Type 0: Not a Combination Product01/11/201810/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH FINALpart34101/11/201810/01/2021
    Labeler - Bi-Mart (027630078)
    Registrant - Aurohealth LLC (078728447)
    Establishment
    NameAddressID/FEIBusiness Operations
    Aurohealth LLC078728447MANUFACTURE(37835-952)

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