Coricidin HBP Maximum Strength Cold, Cough & Flu Liquid Gels, UI1614532

Coricidin HBP Maximum Strength Cold, Cough and Flu by

Drug Labeling and Warnings

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

Drug Details [pdf]

CORICIDIN HBP MAXIMUM STRENGTH COLD, COUGH AND FLU- acetaminophen, dextromethorphan hydrobromide, guaifenesin capsule, liquid filled 
Bayer HealthCare LLC.

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Coricidin HBP Maximum Strength Cold, Cough & Flu Liquid Gels, UI1614532

Drug Facts

Active Ingredients

Active ingredients (in each capsule) Purposes

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

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

Guaifenesin 200 mg…………………………………………...Expectorant

Purpose

Uses

Uses

· temporarily relieves these symptoms due to a cold or flu: · minor aches and pains · headache · cough · sore throat

· helps loosen phlegm ( mucus) and thin bronchial secretions to make cough more productive

· temporarily reduces fever

Warnings

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

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

● in children under 12 years of age

Ask a doctor before use if you have

Ask a doctor before use if you have

● liver disease

● persistent or chronic cough such as occurs with smoking, asthma,

or emphysema

● cough is accompanied by excessive phlegm (mucus)

Ask a doctor or pharmacist

Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin

Stop use and ask a doctor if

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. 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 for children even if you do not notice any signs or symptoms.

Directions

Directions

· do not take more than the recommended dose

· adults and children 12 years and over: take 2 capsules with water

every 4 hours. Do not exceed 10 capsules in 24 hours or as

directed by a doctor.

· children under 12 years of age: do not use

Other information

Other information

● store at 15º-25ºC (59º-77ºF)

Inactive ingredients

Inactive ingredients FD&C red No.40, gelatin, glycerin, iron oxide black, lecithin, medium-chain triglycerides, polyethylene glycol, potassium aluminum silicate, povidone, propylene glycol, purified water, shellac, sodium hydroxide, sorbitol sorbitan solution, titanium dioxide

Questions or comments

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

Package label - 24 count carton

Coricidin®

HBP

COLD RELIEF FOR PEOPLE WITH

HIGH BLOOD PRESSURE Ɨ

MAXIMUM STRENGTH

COLD,

COUGH

& FLU

Relieves

  • Body aches & Pains
  • Headache
  • Fever
  • Cough
  • Sore Throat
  • Chest Congestion

ƗDecongestant Free

24 LIQUID GELS

(Liquid-Filled Capsules)

Carton 24 count

CORICIDIN HBP MAXIMUM STRENGTH COLD, COUGH AND FLU 
acetaminophen, dextromethorphan hydrobromide, guaifenesin capsule, liquid filled
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 11523-0006
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN200 mg
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg
Inactive Ingredients
Ingredient NameStrength
SORBITAN (UNII: 6O92ICV9RU)  
POVIDONE (UNII: FZ989GH94E)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
SORBITOL (UNII: 506T60A25R)  
WATER (UNII: 059QF0KO0R)  
SHELLAC (UNII: 46N107B71O)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
GLYCERIN (UNII: PDC6A3C0OX)  
GELATIN (UNII: 2G86QN327L)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
POTASSIUM ALUMINUM DISILICATE (UNII: SRB14JRX6C)  
Product Characteristics
ColorredScoreno score
ShapeOVALSize20mm
FlavorImprint Code CHBPD
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 11523-0006-12 in 1 CARTON07/01/2020
112 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01207/01/202010/31/2023
Labeler - Bayer HealthCare LLC. (112117283)

Revised: 6/2024
 

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