CORICIDIN HBP MAXIMUM STRENGTH FLU- acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide tablet

Coricidin HBP Maximum Strength Flu by

Drug Labeling and Warnings

Coricidin HBP Maximum Strength Flu by is a Otc medication manufactured, distributed, or labeled by Bayer HealthCare LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients (in each tablet)

Acetaminophen 325 mg

Chlorpheniramine maleate 2 mg

Dextromethorphan hydrobromide 10 mg

Purposes

• 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

• 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: 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 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 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
• glaucoma
• 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

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 beverages
• alcohol, sedatives and tranquilizers may increase drowsiness
• use caution when driving a motor vehicle or operating machinery

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

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

Keep out of reach of children

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.

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 information

• store at room temperature. Avoid excessive heat.

Inactive ingredients

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

Questions or comments?

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

Coricidin HBP Maximum Strength Flu-10 count Carton

NEW FORMULA

Coricidin

HPB

MAXIMUM STRENGTH FLU

DECONGESTATNT-FREE COLD

SYMPTOM RELIEF for people with

HIGH BLOOD PRESSURE

Relieves:

• Body Aches, Pains and headache
• Fever
• Cough
• Runny Nose
• Sore Throat
• Sneezing

Chlorpheniramine maleate / Antihistamine

Dextromethorphan HBr / Cough suppresant

Acetaminophen / Pain reliever-Fever reducer

SEE NEW DOSING DIRECTIONS

American Heart Aassociation

Health Informaiton Enclosed

10 TABLETS

INGREDIENTS AND APPEARANCE

CORICIDIN HBP MAXIMUM STRENGTH FLU 
acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11523-4363
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	325 mg
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	10 mg
CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U)	CHLORPHENIRAMINE MALEATE	2 mg

Inactive Ingredients
Ingredient Name	Strength
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
STEARIC ACID (UNII: 4ELV7Z65AP)
TALC (UNII: 7SEV7J4R1U)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FD&C RED NO. 40 (UNII: WZB9127XOA)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
POVIDONE (UNII: FZ989GH94E)
STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)

Product Characteristics
Color	red	Score	no score
Shape	OVAL	Size	17mm
Flavor		Imprint Code	C;FLU
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11523-4363-1	1 in 1 CARTON	07/20/2018
1		10 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC: 11523-4363-2	2 in 1 CARTON	07/20/2018
2		10 in 1 BLISTER PACK; Type 0: Not a Combination Product
3	NDC: 11523-4363-3	2 in 1 CARTON	07/01/2020
3		12 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	07/20/2018

Labeler - Bayer HealthCare LLC. (112117283)