Label: CORICIDIN HBP MAXIMUM STRENGTH MULTI SYMPTOM FLU- acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide tablet

  • NDC Code(s): 11523-0038-1, 11523-0038-2
  • Packager: Bayer HealthCare LLC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 4, 2025

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

  • SPL UNCLASSIFIED SECTION

    Coricidin HBP

    Maximum Strength Multi-Symptom Flu

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Active ingredients (in each tablet) Purposes

    Acetaminophen 325 mg………………….………….Pain reliever/fever reducer

    Chlorpheniramine maleate 2 mg……….......................................Antihistamine

    Dextromethorphan hydrobromide 10 mg…………………..Cough suppressant

  • PURPOSE

  • Uses

    Uses

    • temporarily relieves these symptoms due to a cold or flu:
    • minor aches and pains
    • headache
    • cough
    • runny nose
    • sneezing
    • sore throat
    • temporarily reduces fever
  • Warnings

    Liver warning

    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

    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

    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
    • trouble urinating due to an enlarged prostate gland
    • cough that occurs with excessive phlegm (mucus)
    • a breathing problem or persistent or chronic cough as occurs with smoking, asthma, chronic bronchitis, or emphysema

    When using this product

    • excitability may occur, especially in children
    • marked drowsiness may occur
    • avoid alcoholic beverages
    • alcohol, sedatives and tranquilizers may increase drowsiness
    • use caution when driving a motor vehicle or operating machinery

    Ask a doctor or pharmacist before use if you are

    • taking the blood thinning drug warfarin
    • taking sedatives or tranquilizers

    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. Abuse of this product can lead to serious injury.

    Overdose warning

    Overdose warning: Taking more than the recommended dose may cause liver damage. In case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical for adults as well as children even if you do not notice any signs or symptoms.

  • DOSAGE & ADMINISTRATION

    Directions

    do not use more than directed (see overdose warning)

    adults and children 12 years and over: take 2 tablets every 4 hours, while symptoms persist. Do not take more than 10 tablets in 24 hours or as directed by a doctor.

    children under 12 years of age: ask a doctor

  • OTHER SAFETY INFORMATION

    Other information

    store at room temperature. Avoid excessive heat.

  • INACTIVE INGREDIENT

    Inactive ingredients FD&C red #40 aluminum lake, lecithin, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, povidone, pregelatinized starch, stearic acid, talc, titanium dioxide

  • QUESTIONS

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

  • Carton

    NDC 11523-0038Coricidin®

    HBP COLD RELIEF FOR PEOPLE WITH

    HIGH BLOOD PRESSUREƗ

    MAXIMUM STRENGTH

    MULTI-SYMPTOM

    FLU

    Relieves

    • Body Aches & Pains
    • Headache
    • Fever
    • Cough
    • Runny Nose & Sneezing
    • Sore Throat

    ƗDecongestant Free

    24 tablets

    Acetaminophen - Pain Reliever/Fever Reducer

    Chlorpheniramine Maleate - Antihistamine

    Dextromethorphan HBr - Cough Supressant

    LEARN MORE

    American Heart Association

    Information Enclosed

  • INGREDIENTS AND APPEARANCE
    CORICIDIN HBP MAXIMUM STRENGTH MULTI SYMPTOM FLU 
    acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11523-0038
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg
    CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE2 mg
    Inactive Ingredients
    Ingredient NameStrength
    TALC (UNII: 7SEV7J4R1U)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    POVIDONE (UNII: FZ989GH94E)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    ColorredScoreno score
    ShapeOVALSize17mm
    FlavorImprint Code c;flu
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11523-0038-11 in 1 CARTON09/04/2020
    110 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:11523-0038-22 in 1 CARTON09/04/2020
    212 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01207/01/2020
    Labeler - Bayer HealthCare LLC. (112117283)