alka-seltzer heartburn relief extra strength

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 relief extra strength
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 1976 mg/1

Manufacturer
Bayer Healthcare LLC

Identifiers & Regulatory

Product NDC 0280-0079
Product ID 0280-0079_30155636-9069-f8ae-e063-6394a90a54a4
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2021-09-21

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 02800079
Hyphenated Format 0280-0079

Supplemental Identifiers

RxCUI
2571087
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 relief extra strength (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
  • 1976 mg/1
source: ndc
Packaging
  • 12 PACKET in 1 CARTON (0280-0079-01) / 2 TABLET, EFFERVESCENT in 1 PACKET
  • 36 PACKET in 1 CARTON (0280-0079-02) / 2 TABLET, EFFERVESCENT in 1 PACKET
  • 18 PACKET in 1 CARTON (0280-0079-03) / 2 TABLET, EFFERVESCENT in 1 PACKET
source: ndc

Packages (3)

Ingredients (2)

citric acid monohydrate (1000 mg/1) sodium bicarbonate (1976 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "30155636-9069-f8ae-e063-6394a90a54a4", "openfda": {"unii": ["2968PHW8QP", "8MDF5V39QO"], "rxcui": ["2571087"], "spl_set_id": ["dc1641f8-54c2-0d86-e053-2995a90a1dce"], "manufacturer_name": ["Bayer Healthcare LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 PACKET in 1 CARTON (0280-0079-01)  / 2 TABLET, EFFERVESCENT in 1 PACKET", "package_ndc": "0280-0079-01", "marketing_start_date": "20210921"}, {"sample": false, "description": "36 PACKET in 1 CARTON (0280-0079-02)  / 2 TABLET, EFFERVESCENT in 1 PACKET", "package_ndc": "0280-0079-02", "marketing_start_date": "20230523"}, {"sample": false, "description": "18 PACKET in 1 CARTON (0280-0079-03)  / 2 TABLET, EFFERVESCENT in 1 PACKET", "package_ndc": "0280-0079-03", "marketing_start_date": "20240401"}], "brand_name": "Alka-Seltzer Heartburn Relief Extra Strength", "product_id": "0280-0079_30155636-9069-f8ae-e063-6394a90a54a4", "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": "0280-0079", "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 Relief Extra Strength", "active_ingredients": [{"name": "CITRIC ACID MONOHYDRATE", "strength": "1000 mg/1"}, {"name": "SODIUM BICARBONATE", "strength": "1976 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210921", "listing_expiration_date": "20261231"}