alka-seltzer heartburn relief extra strength
Generic: anhydrous citric acid, sodium bicarbonate (heat-treated)
Labeler: bayer healthcare llcDrug 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
Active Ingredients
citric acid monohydrate 1000 mg/1, sodium bicarbonate 1976 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
02800079
Hyphenated Format
0280-0079
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 1000 mg/1
- 1976 mg/1
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
Packages (3)
Ingredients (2)
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"}