Alka-Seltzer Heartburn Plus Gas ReliefChews Tropical Punch

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 Heartburn Plus Gas ReliefChews Tropical Punch
Generic name: CALCIUM CARBONATE AND SIMETHICONE
Manufacturer: Bayer HealthCare LLC.
Product type: HUMAN OTC DRUG
SPL set ID: 41d17406-3653-4889-81df-6270b7b5d3c7
SPL ID: 4cd95f62-f7ef-1ef6-e063-6394a90a4d7e
Version: 9
Effective date: 2026-03-12
Source export date: 2026-10-12
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:14:31

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 · 24 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M001	openfda.application_number
brand name		Alka-Seltzer Heartburn Plus Gas ReliefChews Tropical Punch	openfda.brand_name
generic name		CALCIUM CARBONATE AND SIMETHICONE	openfda.generic_name
manufacturer name		Bayer HealthCare LLC.	openfda.manufacturer_name
ndc	package	0280-0225-02	openfda.package_ndc
ndc	package	0280-0225-03	openfda.package_ndc
ndc	package	0280-0225-82	openfda.package_ndc
ndc	package	0280-0225-54	openfda.package_ndc
ndc	package	0280-0225-32	openfda.package_ndc
ndc	package	0280-0225-05	openfda.package_ndc
ndc	package	0280-0225-01	openfda.package_ndc
ndc	product	0280-0225	openfda.product_ndc
ndc11	package	00280022503	derived:openfda.package_ndc
ndc11	package	00280022505	derived:openfda.package_ndc
ndc11	package	00280022582	derived:openfda.package_ndc
ndc11	package	00280022501	derived:openfda.package_ndc
ndc11	package	00280022502	derived:openfda.package_ndc
ndc11	package	00280022532	derived:openfda.package_ndc
ndc11	package	00280022554	derived:openfda.package_ndc
rxcui		1492387	openfda.rxcui
spl id		4cd95f62-f7ef-1ef6-e063-6394a90a4d7e	id
spl set id		41d17406-3653-4889-81df-6270b7b5d3c7	set_id
unii		H0G9379FGK	openfda.unii
unii		92RU3N3Y1O	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 6 chewable tablets 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 constipation may occur If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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