Alka-Seltzer Cool Action Heartburn Relief Mint

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Alka-Seltzer Cool Action Heartburn Relief Mint
Generic name: CALCIUM CARBONATE
Manufacturer: Bayer HealthCare LLC.
Product type: HUMAN OTC DRUG
SPL set ID: 9b8da147-8d0c-e6b0-e053-2a95a90a35e6
SPL ID: 452374f2-bab8-ec4e-e063-6294a90adca9
Version: 7
Effective date: 2025-12-04
Source export date: 2026-10-27
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:58:36

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M001	openfda.application_number
brand name		Alka-Seltzer Cool Action Heartburn Relief Mint	openfda.brand_name
generic name		CALCIUM CARBONATE	openfda.generic_name
manufacturer name		Bayer HealthCare LLC.	openfda.manufacturer_name
ndc	package	0280-0001-01	openfda.package_ndc
ndc	package	0280-0001-03	openfda.package_ndc
ndc	package	0280-0001-04	openfda.package_ndc
ndc	package	0280-0001-02	openfda.package_ndc
ndc	product	0280-0001	openfda.product_ndc
ndc11	package	00280000101	derived:openfda.package_ndc
ndc11	package	00280000102	derived:openfda.package_ndc
ndc11	package	00280000104	derived:openfda.package_ndc
ndc11	package	00280000103	derived:openfda.package_ndc
rxcui		2281777	openfda.rxcui
spl id		452374f2-bab8-ec4e-e063-6294a90adca9	id
spl set id		9b8da147-8d0c-e6b0-e053-2a95a90a35e6	set_id
unii		H0G9379FGK	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Do not use if you have ever had an allergic reaction to this product or any of its ingredients Ask a doctor or pharmacist before use if you are presently taking a prescription drug. Antacids may interact with certain prescription drugs. When using this product ● do not use more than 5 pieces in a 24-hour period ● if pregnant do not use more than 5 pieces in a 24-hour period ● do not use the maximum dosage of this product for more than 2 weeks except under the advice and supervision of a physician If pregnant or breast-feeding, inform your doctor that you are using this product. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.