TUMS ULTRA

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: TUMS ULTRA
Generic name: CALCIUM CARBONATE
Manufacturer: Haleon US Holdings LLC
Product type: HUMAN OTC DRUG
SPL set ID: f4786707-a0f7-4ba8-9656-06278d1b4b6c
SPL ID: 5607f6ca-b124-ff93-e063-6394a90a6de3
Version: 20
Effective date: 2026-07-07
Source export date: 2026-09-28
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/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:55:49

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 2 · 54 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M001	openfda.application_number
brand name		TUMS ULTRA	openfda.brand_name
generic name		CALCIUM CARBONATE	openfda.generic_name
manufacturer name		Haleon US Holdings LLC	openfda.manufacturer_name
ndc	package	0135-0540-01	openfda.package_ndc
ndc	package	0135-0228-01	openfda.package_ndc
ndc	package	0135-0181-02	openfda.package_ndc
ndc	package	0135-0181-01	openfda.package_ndc
ndc	package	0135-0118-14	openfda.package_ndc
ndc	package	0135-0181-06	openfda.package_ndc
ndc	package	0135-0228-05	openfda.package_ndc
ndc	package	0135-0180-14	openfda.package_ndc
ndc	package	0135-0181-05	openfda.package_ndc
ndc	package	0135-0228-04	openfda.package_ndc
ndc	package	0135-0181-07	openfda.package_ndc
ndc	package	0135-0228-07	openfda.package_ndc
ndc	package	0135-0181-03	openfda.package_ndc
ndc	package	0135-0228-06	openfda.package_ndc
ndc	package	0135-0180-02	openfda.package_ndc
ndc	package	0135-0180-01	openfda.package_ndc
ndc	package	0135-0118-01	openfda.package_ndc
ndc	package	0135-0181-14	openfda.package_ndc
ndc	package	0135-0118-83	openfda.package_ndc
ndc	package	0135-0118-04	openfda.package_ndc
ndc	product	0135-0118	openfda.product_ndc
ndc	product	0135-0540	openfda.product_ndc
ndc	product	0135-0228	openfda.product_ndc
ndc	product	0135-0181	openfda.product_ndc
ndc	product	0135-0180	openfda.product_ndc
ndc11	package	00135011804	derived:openfda.package_ndc
ndc11	package	00135018102	derived:openfda.package_ndc
ndc11	package	00135018002	derived:openfda.package_ndc
ndc11	package	00135022804	derived:openfda.package_ndc
ndc11	package	00135018103	derived:openfda.package_ndc
ndc11	package	00135011883	derived:openfda.package_ndc
ndc11	package	00135022801	derived:openfda.package_ndc
ndc11	package	00135022806	derived:openfda.package_ndc
ndc11	package	00135018001	derived:openfda.package_ndc
ndc11	package	00135018101	derived:openfda.package_ndc
ndc11	package	00135018114	derived:openfda.package_ndc

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 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 7 tablets in 24 hours if pregnant do not take more than 5 tablets in 24 hours do not use the maximum dosage for more than 2 weeks, except under the advice and supervision of a doctor Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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