Sodium Bicarbonate

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: Sodium Bicarbonate
Generic name: SODIUM BICARBONATE
Manufacturer: Cardinal Health 107, LLC
Product type: HUMAN OTC DRUG
SPL set ID: f7c88834-aa7c-4aaa-ab9b-0cbcd1f4da3f
SPL ID: 73bf9e65-e5f5-4439-b4cf-a9e43214280e
Version: 6
Effective date: 2024-11-07
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:18:03

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Sodium Bicarbonate	openfda.brand_name
generic name		SODIUM BICARBONATE	openfda.generic_name
manufacturer name		Cardinal Health 107, LLC	openfda.manufacturer_name
ndc	package	55154-6754-0	openfda.package_ndc
ndc	product	55154-6754	openfda.product_ndc
ndc11	package	55154675400	derived:openfda.package_ndc
rxcui		198861	openfda.rxcui
spl id		73bf9e65-e5f5-4439-b4cf-a9e43214280e	id
spl set id		f7c88834-aa7c-4aaa-ab9b-0cbcd1f4da3f	set_id
unii		8MDF5V39QO	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 This Unit Dose package is not child resistant and is Intended for Institutional Use Only. Do not take more than 24 tablets for adults up to 60 years of age (or 12 tablets for adults 60 years of age and older) in a 24-hour period nor use the maximum dosage for more than 2 weeks, except under the advice and supervision of a physician. Ask a doctor before use if you have a sodium restricted diet. Ask a doctor or pharmacist before use if you are taking a prescription drug. Antacids may interact with certain prescription drugs. Stop use and ask a doctor if symptoms last more than 2 weeks. If you are pregnant or breast-feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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