Alka-Seltzer Cool Action Extra Strength ReliefChews 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 Extra Strength ReliefChews Mint
Generic name: CALCIUM CARBONATE
Manufacturer: Bayer HealthCare LLC.
Product type: HUMAN OTC DRUG
SPL set ID: 849bd52a-b730-3ba7-e053-2a91aa0a507c
SPL ID: 45262c76-563b-6aee-e063-6394a90af808
Version: 6
Effective date: 2025-12-04
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:19:08

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 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M001	openfda.application_number
brand name		Alka-Seltzer Cool Action Extra Strength ReliefChews Mint	openfda.brand_name
generic name		CALCIUM CARBONATE	openfda.generic_name
manufacturer name		Bayer HealthCare LLC.	openfda.manufacturer_name
ndc	package	0280-0058-50	openfda.package_ndc
ndc	package	0280-0058-30	openfda.package_ndc
ndc	product	0280-0058	openfda.product_ndc
ndc11	package	00280005850	derived:openfda.package_ndc
ndc11	package	00280005830	derived:openfda.package_ndc
rxcui		308915	openfda.rxcui
spl id		45262c76-563b-6aee-e063-6394a90af808	id
spl set id		849bd52a-b730-3ba7-e053-2a91aa0a507c	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 take more than 5 chewable tablets in a 24-hour period ● if pregnant do not take more than 5 tablets in 24 hours ● 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.