Coricidin HBP Maximum Strength Multi Symptom Flu

Manufacturer
Bayer HealthCare LLC.
Effective date
2025-12-04
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:20:01

Label at a glance#

ProductCoricidin HBP Maximum Strength Multi Symptom Flu
Active ingredientDEXTROMETHORPHAN HYDROBROMIDE, ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE
Label structure10 sections

Indications and 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

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Coricidin HBP

Maximum Strength Multi-Symptom Flu

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active ingredients (in each tablet) Purposes

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

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

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

Uses

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

Liver warning

WARNINGS SECTION

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

WARNINGS SECTION

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

OTC - ACTIVE INGREDIENT SECTION

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.

OTC - DO NOT USE SECTION

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

OTC - ASK DOCTOR SECTION

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

OTC - WHEN USING SECTION

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

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if you are

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

OTC - STOP USE SECTION

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.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Abuse of this product can lead to serious injury.

Overdose warning

WARNINGS SECTION

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 SECTION

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 SECTION

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

OTC - QUESTIONS SECTION

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

Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 11523-0038NDC 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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2049841acetaminophen 325 MG / chlorpheniramine maleate 2 MG / dextromethorphan HBr 10 MG Oral TabletPSN5
2049841acetaminophen 325 MG / chlorpheniramine maleate 2 MG / dextromethorphan hydrobromide 10 MG Oral TabletSCD5
2049841acetaminophen 325 MG / chlorpheniramine maleate 2 MG / dextromethorphan HBr 10 MG Oral TabletSY5
2049841APAP 325 MG / Chlorpheniramine Maleate 2 MG / Dextromethorphan Hydrobromide 10 MG Oral TabletSY5

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CHLORPHENIRAMINE Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813
DEXTROMETHORPHAN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d17a97fa-387f-690e-d2be-0083ab044a03Product name320170725
0fdb98e2-b951-a1ce-5715-2b187ba500efProduct name420170718
c6fba691-a132-4ede-95c6-f8c6bd696636Product name120150902
c0200ab5-4954-454e-9676-30b741b245bdProduct name120150730

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11523-0038-1Coricidin HBP Maximum Strength Multi Symptom Flu10 in 1 BLISTER PACKTABLET105
11523-0038-1Coricidin HBP Maximum Strength Multi Symptom Flu1 in 1 CARTONTABLET15
11523-0038-2Coricidin HBP Maximum Strength Multi Symptom Flu2 in 1 CARTONTABLET25
11523-0038-2Coricidin HBP Maximum Strength Multi Symptom Flu12 in 1 BLISTER PACKTABLET125

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11523-003811523-0038-1, 11523-0038-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Coricidin HBP Maximum Strength Multi Symptom FluACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDEBayer HealthCare LLC.ae7cf41e-b618-d6bb-e053-2a95a90a66922025-12-04WarningsExact identifier
ndc (package): 11523-0038-2
ndc (package): 11523-0038-1
ndc (product): 11523-0038
ndc11 (package): 11523003802
ndc11 (package): 11523003801
spl id: 4526cd5e-1ddf-e13d-e063-6294a90a9531
spl set id: ae7cf41e-b618-d6bb-e053-2a95a90a6692

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.