alka-seltzer heartburn

Generic: anhydrous citric acid, sodium bicarbonate (heat-treated)

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

Drug Facts

Product Profile

Brand Name alka-seltzer heartburn
Generic Name anhydrous citric acid, sodium bicarbonate (heat-treated)
Labeler bayer healthcare llc.
Dosage Form TABLET, EFFERVESCENT
Routes
ORAL
Active Ingredients

citric acid monohydrate 1000 mg/1, sodium bicarbonate 1940 mg/1

Manufacturer
Bayer HealthCare LLC.

Identifiers & Regulatory

Product NDC 0280-0047
Product ID 0280-0047_45261b62-1428-8c69-e063-6294a90a011f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2010-03-02

Pharmacologic Class

Classes
acidifying activity [moa] anti-coagulant [epc] calcium chelating activity [moa] calculi dissolution agent [epc] decreased coagulation factor activity [pe] increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02800047
Hyphenated Format 0280-0047

Supplemental Identifiers

RxCUI
1536470
UNII
2968PHW8QP 8MDF5V39QO

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 heartburn (source: ndc)
Generic Name anhydrous citric acid, sodium bicarbonate (heat-treated) (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
  • 1940 mg/1
source: ndc
Packaging
  • 18 POUCH in 1 CARTON (0280-0047-36) / 2 TABLET, EFFERVESCENT in 1 POUCH
source: ndc

Packages (1)

0280-0047-36 18 POUCH in 1 CARTON (0280-0047-36) / 2 TABLET, EFFERVESCENT in 1 POUCH

Ingredients (2)

citric acid monohydrate (1000 mg/1) sodium bicarbonate (1940 mg/1)

Linked Drug Pages (1)

Alka-Seltzer Heartburn ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45261b62-1428-8c69-e063-6294a90a011f", "openfda": {"unii": ["2968PHW8QP", "8MDF5V39QO"], "rxcui": ["1536470"], "spl_set_id": ["55158e50-0327-2043-e054-00144ff8d46c"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "18 POUCH in 1 CARTON (0280-0047-36)  / 2 TABLET, EFFERVESCENT in 1 POUCH", "package_ndc": "0280-0047-36", "marketing_start_date": "20100302"}], "brand_name": "Alka-Seltzer Heartburn", "product_id": "0280-0047_45261b62-1428-8c69-e063-6294a90a011f", "dosage_form": "TABLET, EFFERVESCENT", "pharm_class": ["Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "0280-0047", "generic_name": "Anhydrous citric acid, Sodium bicarbonate (heat-treated)", "labeler_name": "Bayer HealthCare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Heartburn", "active_ingredients": [{"name": "CITRIC ACID MONOHYDRATE", "strength": "1000 mg/1"}, {"name": "SODIUM BICARBONATE", "strength": "1940 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20100302", "listing_expiration_date": "20261231"}