coricidin hbp day and night

Generic: dextromethorphan hydrobromide, guaifenesin, acetaminophen, chlorpheniramine maleate

Labeler: bayer healthcare llc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name coricidin hbp day and night
Generic Name dextromethorphan hydrobromide, guaifenesin, acetaminophen, chlorpheniramine maleate
Labeler bayer healthcare llc.
Dosage Form KIT
Manufacturer
Bayer HealthCare LLC.

Identifiers & Regulatory

Product NDC 11523-4765
Product ID 11523-4765_45370b45-6102-a96f-e063-6294a90a1721
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2009-08-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 115234765
Hyphenated Format 11523-4765

Supplemental Identifiers

RxCUI
1098496 1111663 1250983

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name coricidin hbp day and night (source: ndc)
Generic Name dextromethorphan hydrobromide, guaifenesin, acetaminophen, chlorpheniramine maleate (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 10 mg
  • 200 mg
  • 500 mg
  • 2 mg
  • 15 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (11523-4765-1) * 2 BLISTER PACK in 1 CARTON (11523-4221-1) / 8 CAPSULE, GELATIN COATED in 1 BLISTER PACK * 2 BLISTER PACK in 1 CARTON (11523-4111-1) / 4 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

11523-4765-1 1 KIT in 1 CARTON (11523-4765-1) * 2 BLISTER PACK in 1 CARTON (11523-4221-1) / 8 CAPSULE, GELATIN COATED in 1 BLISTER PACK * 2 BLISTER PACK in 1 CARTON (11523-4111-1) / 4 TABLET in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Coricidin HBP Day and Night ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "45370b45-6102-a96f-e063-6294a90a1721", "openfda": {"rxcui": ["1098496", "1111663", "1250983"], "spl_set_id": ["e33f2319-2181-46db-a094-3e874b324c0a"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (11523-4765-1)  *  2 BLISTER PACK in 1 CARTON (11523-4221-1)  / 8 CAPSULE, GELATIN COATED in 1 BLISTER PACK *  2 BLISTER PACK in 1 CARTON (11523-4111-1)  / 4 TABLET in 1 BLISTER PACK", "package_ndc": "11523-4765-1", "marketing_start_date": "20090828"}], "brand_name": "Coricidin HBP Day and Night", "product_id": "11523-4765_45370b45-6102-a96f-e063-6294a90a1721", "dosage_form": "KIT", "product_ndc": "11523-4765", "generic_name": "Dextromethorphan Hydrobromide, Guaifenesin, Acetaminophen, Chlorpheniramine maleate", "labeler_name": "Bayer HealthCare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Coricidin HBP", "brand_name_suffix": "Day and Night", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20090828", "listing_expiration_date": "20261231"}