CORICIDIN HBP CHEST CONGESTION AND COUGH- dextromethorphan hydrobromide and guaifenesin capsule, gelatin coated

Coricidin HBP Chest Congestion And Cough by

Drug Labeling and Warnings

Coricidin HBP Chest Congestion And Cough by is a Otc medication manufactured, distributed, or labeled by Bayer HealthCare LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

PURPOSE

• Active ingredients (in each capsule): Purpose
• Dextromethorphan hydrobromide 10 mg: Cough suppressant
• Guaifenesin 200 mg: Expectorant

Uses

• temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold
• helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive

Warnings

Do not use

• 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

• cough that occurs with excessive phlegm (mucus)
• persistent or chronic cough as occurs with smoking, asthma, chronic bronchitis, or emphysema

Stop use and ask a doctor if cough lasts more than 7 days, reoccurs, or occurs with fever, rash or persistent headache. 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. In case of overdose, get medical help or contact a Poison Control Center right away. Abuse of this product can lead to serious injury.

Directions

• do not exceed recommended dose
• adults and children 12 years and over:
  
  1 or 2 capsules every 4 hours, not more than
  
  12 capsules in 24 hours
• children under 12 years of age: ask a doctor

Other information

• store between 20° to 25°C (68° to 77°F)
• protect from freezing
• protect from excessive moisture

Inactive ingredients

FD&C red no. 40, gelatin, glycerin, polyethylene glycol, povidone, propylene glycol, purified water, shellac, sodium, sorbitol sorbitan solution, titanium dioxide.

Questions or comments?

Call 1-800-317-2165 between 8:00 AM and 5:00 PM Central Standard Time, Monday through Friday

PRINCIPAL DISPLAY PANEL - 2 x 10 Softgel Blister Pack Carton

Coricidin ®
HBP

COLD SYMPTOM RELIEF for people with

HIGH BLOOD PRESSURE

CHEST
CONGESTION
& COUGH

Relieves:

• Chest Congestion
• Cough

Guaifenesin - Expectorant,

Dextromethorphan hydrobromide -

cough suppressent

CONTROLS COUGH

FAST

Liqui-Gels ®

DECONGESTANT-FREE

American Heart Association

Health Information Enclosed

20 LIQUID GELS

(Liquid Filled Capsules)

INGREDIENTS AND APPEARANCE

CORICIDIN HBP CHEST CONGESTION AND COUGH 
dextromethorphan hydrobromide and guaifenesin capsule, gelatin coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11523-7158
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	10 mg
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	200 mg

Inactive Ingredients
Ingredient Name	Strength
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SHELLAC (UNII: 46N107B71O)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
SORBITAN (UNII: 6O92ICV9RU)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FD&C RED NO. 40 (UNII: WZB9127XOA)
GELATIN (UNII: 2G86QN327L)
GLYCERIN (UNII: PDC6A3C0OX)
POVIDONE (UNII: FZ989GH94E)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SORBITOL (UNII: 506T60A25R)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	red	Score	no score
Shape	OVAL	Size	20mm
Flavor		Imprint Code	C;HBP
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11523-7158-2	2 in 1 CARTON	08/31/2000	04/30/2022
1		10 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	08/31/2000	04/30/2022

Labeler - Bayer HealthCare LLC. (112117283)