Label: CORICIDIN HBP CHEST CONGESTION AND COUGH- dextromethorphan hydrobromide and guaifenesin capsule, gelatin coated
- NDC Code(s): 11523-7158-2
- Packager: Bayer HealthCare LLC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 5, 2025
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- Uses
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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
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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PRINCIPAL DISPLAY PANEL - 2 x 10 Softgel Blister Pack Carton
Coricidin ®
HBP
COLD SYMPTOM RELIEF for people with
HIGH BLOOD PRESSURECHEST
CONGESTION
& COUGHRelieves:
- Chest Congestion
- Cough
Guaifenesin - Expectorant,
Dextromethorphan hydrobromide -
cough suppressent
CONTROLS COUGH
FASTLiqui-Gels ®
DECONGESTANT-FREE
American Heart Association
Health Information Enclosed
20 LIQUID GELS
(Liquid Filled Capsules)

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INGREDIENTS AND APPEARANCE
CORICIDIN HBP CHEST CONGESTION AND COUGH
dextromethorphan hydrobromide and guaifenesin capsule, gelatin coatedProduct 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 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 Drug M012 08/31/2000 Labeler - Bayer HealthCare LLC. (112117283)
