alka-seltzer plus cough and sore throat fizzychews

Generic: acetaminophen, dextromethorphan hydrobromide

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

Drug Facts

Product Profile

Brand Name alka-seltzer plus cough and sore throat fizzychews
Generic Name acetaminophen, dextromethorphan hydrobromide
Labeler bayer healthcare llc.
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

acetaminophen 162.5 mg/1, dextromethorphan hydrobromide 5 mg/1

Manufacturer
Bayer HealthCare LLC.

Identifiers & Regulatory

Product NDC 0280-0152
Product ID 0280-0152_452660a4-50ec-ef65-e063-6294a90ad533
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2024-04-01

Pharmacologic Class

Classes
sigma-1 agonist [epc] sigma-1 receptor agonists [moa] uncompetitive n-methyl-d-aspartate receptor antagonist [epc] uncompetitive nmda receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02800152
Hyphenated Format 0280-0152

Supplemental Identifiers

RxCUI
2678223
UPC
0016500601715
UNII
362O9ITL9D 9D2RTI9KYH

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 alka-seltzer plus cough and sore throat fizzychews (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 162.5 mg/1
  • 5 mg/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (0280-0152-01) / 8 TABLET, CHEWABLE in 1 BLISTER PACK
  • 3 BLISTER PACK in 1 CARTON (0280-0152-02) / 8 TABLET, CHEWABLE in 1 BLISTER PACK
source: ndc

Packages (2)

Ingredients (2)

acetaminophen (162.5 mg/1) dextromethorphan hydrobromide (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "452660a4-50ec-ef65-e063-6294a90ad533", "openfda": {"upc": ["0016500601715"], "unii": ["362O9ITL9D", "9D2RTI9KYH"], "rxcui": ["2678223"], "spl_set_id": ["14951faa-9476-6f29-e063-6394a90a14c7"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0280-0152-01)  / 8 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "0280-0152-01", "marketing_start_date": "20240401"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (0280-0152-02)  / 8 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "0280-0152-02", "marketing_start_date": "20240401"}], "brand_name": "Alka-Seltzer Plus Cough and Sore Throat FizzyChews", "product_id": "0280-0152_452660a4-50ec-ef65-e063-6294a90ad533", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "0280-0152", "generic_name": "acetaminophen, dextromethorphan hydrobromide", "labeler_name": "Bayer HealthCare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Plus Cough and Sore Throat FizzyChews", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "162.5 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240401", "listing_expiration_date": "20261231"}