Label: CORICIDIN HBP NIGHTTIME MULTI-SYMPTOM COLD- acetaminophen,dextromethorphan hydrobromide, doxylamine succinate liquid

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

Drug Label Information

Updated November 30, 2023

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  • Drug Facts

  • Active ingredients (in each 15 mL)

    Acetaminophen 325 mgPain reliever/fever reducer
    Dextromethorphan hydrobromide 15 mgCough suppresant
    Doxylamine succinate 6.25 mgAntihistamine

  • Purpose

    Acetaminophen 325 mgPain reliever/fever reducer
    Dextromethorphan hydrobromide 15 mgCough suppresant
    Doxylamine succinate 6.25 mgAntihistamine

  • Uses

    temporarily relieves common cold/flu symptoms:

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

    Liver warning

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

    • more than 120 mL (4 doses) in 24 hours, which is the maximum daily amount
    • with other drugs containing acetaminophen
    • 3 or more alcoholic drinks every day while using this product

    Allergy alert

    acetaminophen may cause severe skin or severe allergic reactions. Symptoms may include:

    • skin reddening
    • blisters
    • rash
    • hives
    • facial swelling
    • asthma (wheezing)
    • shock

    If a skin or general allergic 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 note use

    • with any other products containing acetaminophen (prescription or nonprescription). If you are no 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.
  • Ask a doctor before use if you have

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

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

    • 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

    • fever gets worse or lasts more than 3 days
    • cough comes back or occurs with rash or headache that lasts. These could be signs of a serious condition.
    • pain, cough, or nasal congestion gets worse or lasts more than 7 days
    • new symptoms occur
    • redness or swelling is present
  • If pregnant or breast-feeding

    If pregnant or breast-feeding, ask a health professional before use.

  • Keep out of reach of children

    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

    • do not take more than directed
    • adults and children 12 years and over: take 30 mL in the dosing cup provided every 6 hours while symptoms last
    • do not exceed 120 mL (4 doses) in 24 hours, unless directed by a doctor
    • children under 12 years: ask a doctor
  • Other information

    • each 15 mL contains: sodium 18 mg
    • store at 20º-25ºC (68º-77ºF)
  • Inactive ingredients

    alcohol 10%, anhydrous citric acid, FD&C blue no.1, FD&C red no.40, flavor, high fructose corn syrup, polyethylene glycol, propylene glycol, purified water, saccharin sodium, sodium citrate

  • Questions or comments

    Questions or comments? 1-800-317-2165 (Mon – Fri 9AM – 5PM EST)

  • PRINCIPAL DISPLAY PANEL

    nighttimeliq

  • INGREDIENTS AND APPEARANCE
    CORICIDIN HBP NIGHTTIME MULTI-SYMPTOM COLD 
    acetaminophen,dextromethorphan hydrobromide, doxylamine succinate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11523-4358
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DOXYLAMINE SUCCINATE (UNII: V9BI9B5YI2) (DOXYLAMINE - UNII:95QB77JKPL) DOXYLAMINE SUCCINATE6.25 mg  in 15 mL
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg  in 15 mL
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE15 mg  in 15 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorCHERRYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11523-4358-1355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/20/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01211/20/2015
    Labeler - Bayer HealthCare LLC. (112117283)
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