TUMS Smoothies

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 Smoothies
Generic name: CALCIUM CARBONATE
Manufacturer: Haleon US Holdings LLC
Product type: HUMAN OTC DRUG
SPL set ID: c22944b8-8733-4689-be0c-f320467f79ea
SPL ID: 4e6d1e5b-2025-907d-e063-6294a90abe8c
Version: 21
Effective date: 2026-04-01
Source export date: 2026-09-28
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:39:28

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 · 38 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M001	openfda.application_number
brand name		TUMS Smoothies	openfda.brand_name
generic name		CALCIUM CARBONATE	openfda.generic_name
manufacturer name		Haleon US Holdings LLC	openfda.manufacturer_name
ndc	package	0135-0246-01	openfda.package_ndc
ndc	package	0135-0456-03	openfda.package_ndc
ndc	package	0135-0221-01	openfda.package_ndc
ndc	package	0135-0246-05	openfda.package_ndc
ndc	package	0135-0456-01	openfda.package_ndc
ndc	package	0135-0246-07	openfda.package_ndc
ndc	package	0135-0246-04	openfda.package_ndc
ndc	package	0135-0456-05	openfda.package_ndc
ndc	package	0135-0243-02	openfda.package_ndc
ndc	package	0135-0246-02	openfda.package_ndc
ndc	package	0135-0456-04	openfda.package_ndc
ndc	package	0135-0245-02	openfda.package_ndc
ndc	product	0135-0243	openfda.product_ndc
ndc	product	0135-0221	openfda.product_ndc
ndc	product	0135-0456	openfda.product_ndc
ndc	product	0135-0246	openfda.product_ndc
ndc	product	0135-0245	openfda.product_ndc
ndc11	package	00135024607	derived:openfda.package_ndc
ndc11	package	00135024601	derived:openfda.package_ndc
ndc11	package	00135024602	derived:openfda.package_ndc
ndc11	package	00135024605	derived:openfda.package_ndc
ndc11	package	00135024302	derived:openfda.package_ndc
ndc11	package	00135045603	derived:openfda.package_ndc
ndc11	package	00135045601	derived:openfda.package_ndc
ndc11	package	00135022101	derived:openfda.package_ndc
ndc11	package	00135024502	derived:openfda.package_ndc
ndc11	package	00135045605	derived:openfda.package_ndc
ndc11	package	00135024604	derived:openfda.package_ndc
ndc11	package	00135045604	derived:openfda.package_ndc
rxcui		1044532	openfda.rxcui
rxcui		308915	openfda.rxcui
spl id		4e6d1e5b-2025-907d-e063-6294a90abe8c	id
spl set id		c22944b8-8733-4689-be0c-f320467f79ea	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 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 10 tablets in 24 hours if pregnant do not take more than 6 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.