Sodium Bicarbonate Antacid

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 Antacid
Generic name: SODIUM BICARBONATE
Manufacturer: Menper Distributors Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 6efb4da0-03ae-4df6-acd7-e8023d20d4b3
SPL ID: 3a8afea2-5d9e-1392-e063-6294a90aca43
Version: 3
Effective date: 2025-07-22
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 05:20:36

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 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M001	openfda.application_number
brand name		Sodium Bicarbonate Antacid	openfda.brand_name
generic name		SODIUM BICARBONATE	openfda.generic_name
manufacturer name		Menper Distributors Inc.	openfda.manufacturer_name
ndc	package	53145-390-04	openfda.package_ndc
ndc	package	53145-390-08	openfda.package_ndc
ndc	package	53145-390-16	openfda.package_ndc
ndc	product	53145-390	openfda.product_ndc
ndc11	package	53145039016	derived:openfda.package_ndc
ndc11	package	53145039008	derived:openfda.package_ndc
ndc11	package	53145039004	derived:openfda.package_ndc
spl id		3a8afea2-5d9e-1392-e063-6294a90aca43	id
spl set id		6efb4da0-03ae-4df6-acd7-e8023d20d4b3	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 FOR ORAL USE ONLY STOMACH WARNING: TO AVOID SERIOUS INJURY, DO NOT TAKE UNTIL POWDER IS COMPLETELY DISSOLVED. IT IS VERY IMPORTANT NOT TO TAKE THIS PRODUCT WHEN OVERLY FILL FROM FOOD OR DRINK. Do not use in children under 12 years of age. Ask a doctor or pharmacist before use if you have a sodium-restricted diet. Ask a doctor or pharmacist before use if you are presently taking a prescription drug. Antacids may interact with certain prescription drugs. Stop use and ask a doctor if you have used the maximum dosage for 2 wekks sever stomach pain occurs after using this product

Reported adverse events (FAERS/openFDA)#

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