Sodium Bicarbonate

Product NDC: 69367-258
11-digit product format: 693670258
Labeler code: 69367
Product ID: 69367-258_43b42880-bab8-4580-8a00-ae13855d44a3
Type: HUMAN OTC DRUG
Nonproprietary name: Sodium Bicarbonate
Dosage form: TABLET
Route: ORAL
Labeler: Westminster Pharmaceuticals, LLC
Application: M001
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2022-10-10
Substance: SODIUM BICARBONATE
Active strength: 650 mg/1
Pharmacologic classes: Alkalinizing Activity [MoA]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Sodium Bicarbonate
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SODIUM BICARBONATE	650 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
8MDF5V39QO	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
198861	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
9dcfc778-5fd6-4c68-8d37-a5385e374617	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
fb7ab793-2c12-4079-b100-a64f73bef25a	Product name	4	20240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7	Product name	2	20230717
dc7c5daa-021f-40dd-b00d-63982cb2067a	Product name	1	20230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	5	20200925
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	2	20160823
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69367-258-10	Sodium Bicarbonate	1000 in 1 BOTTLE	TABLET	1000		10

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
69367-258-10	EA - Each	69367-258	a1b249a4-e5e5-4321-8168-8cc6532ba91d	1	2022-11-07

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69367-258	SODIUM BICARBONATE TABLET [WESTMINSTER PHARMACEUTICALS, LLC]	9	Current NDC, Legacy NDC, 1 package rows	20250425_9dcfc778-5fd6-4c68-8d37-a5385e374617.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 30 of 34 · 678 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Goodsense Extra Strength Antacid	CALCIUM CARBONATE	GoodSense	193a1805-9f57-29cd-e063-6394a90ab99f	2024-09-13	Warnings	Exact identifier application number: M001
QCH Maximum Strength Antacid 516	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE	Chain Drug Marketing Association Inc.	1794c35a-79c5-48c2-e063-6394a90a6d29	2024-08-28	Warnings	Exact identifier application number: M001
QCH Regular Strength Antacid 509	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE	Chain Drug Marketing Association Inc.	17947ccd-6f11-d4cd-e063-6294a90a108a	2024-08-27	Warnings	Exact identifier application number: M001
Regular Strength Antacid Antigas	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE	Chain Drug Marketing Association Inc.	17dfe539-923b-e623-e063-6294a90a041f	2024-08-27	Warnings	Exact identifier application number: M001
QCH Extra Strength Gas Relief Cherry Flavor 134CHR	SIMETHICONE	Chain Drug Marketing Association Inc.	17e3300c-3d31-b7e1-e063-6294a90af082	2024-08-27	Warnings	Exact identifier application number: M001
Quality Choice Infants Non-staining Gas relief	SIMETHICONE	Chain Drug Marketing Association Inc.	17e181e5-6527-54d0-e063-6294a90addc2	2024-08-23	Warnings	Exact identifier application number: M001
Tums Chewy Bites	CALCIUM CARBONATE	Haleon US Holdings LLC	72ac000c-90f7-42e2-88a6-740de114a954	2024-08-21	Warnings	Exact identifier application number: M001
GDC Extra strength Alkums Antacid 127AF	CALCIUM CARBONATE	Guardian Drug Company	1b6da4a3-cfa6-6d98-e063-6394a90a5889	2024-08-13	Warnings	Exact identifier application number: M001
Wonderbelly Maximum Strength Antacid - Sweet Mint	CALCIUM CARBONATE	Ginger Health Company	17ddf76b-237a-eeee-e063-6294a90ac205	2024-07-29	Warnings	Exact identifier application number: M001
Good Neighbor Pharmacy Antacid Regular Strength	CALCIUM CARBONATE	AmerisourceBergen Drug Corporation	2847e82e-203e-4976-8c4f-4a5caa75ce00	2024-07-09	Warnings	Exact identifier application number: M001
Kirkland Ultra Stregth Antacid 171AB	CALCIUM CARBONATE	COSTCO WHOLESALE COMPANY	1bea92e8-1b94-77b0-e063-6394a90a8212	2024-07-08	Warnings	Exact identifier application number: M001
ANTACID AND GASRELIEF	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	GOODSENSE	a951fa64-7775-470e-e053-2995a90aefc4	2024-06-10	Warnings	Exact identifier application number: M001
MINTOX MAXIMUM STRENGTH	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	NuCare Pharmaceuticals,Inc.	5b1f4c78-d42e-32c7-e053-2991aa0a1985	2024-06-04	Warnings	Exact identifier application number: M001
Mylanta All-Family Multi Symptom Stomach Remedy	CALCIUM CARBONATE, SIMETHICONE	Infirst Healthcare Inc.	19118884-2016-e86e-e063-6294a90a370c	2024-05-22	Warnings	Exact identifier application number: M001
Stomach Circle K	BISMUTH SUBSALICYLATE	Lil' Drug Store Products, Inc	05e14009-b35d-4711-b6f0-89b6d060b387	2024-05-06	Warnings	Exact identifier application number: M001
Tums Chewy Bites Peppermint	CALCIUM CARBONATE	Haleon US Holdings LLC	45a44b2b-1633-49c5-8c55-9e9af3545c92	2024-05-03	Warnings	Exact identifier application number: M001
MINT ANTACID 100	CALCIUM CARBONATE	JHK Inc dba American Safety & First Aid	2496aed6-68ec-44c4-afc9-f7fa41b2147b	2024-04-24	Warnings	Exact identifier application number: M001
Tums Chewy Bites Assorted Berries	CALCIUM CARBONATE	Navajo Manufacturing Company Inc.	1625c724-7ead-cc70-e063-6294a90aa558	2024-04-15	Warnings	Exact identifier application number: M001
Gas-X Maximum Strength Softgels	SIMETHICONE	Haleon US Holdings LLC	45d1e373-0717-47df-9160-619c451666f4	2024-04-05	Warnings	Exact identifier application number: M001
Gas-X Total Relief Maximum Strength	CALCIUM CARBONATE, SIMETHICONE	Haleon US Holdings LLC	62fc0a91-c44f-4546-a472-c183a2d95486	2024-04-05	Warnings	Exact identifier application number: M001

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
8MDF5V39QO	SODIUM BICARBONATE	144-55-8	SODIUM BICARBONATE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
198861	sodium bicarbonate 650 MG Oral Tablet	PSN	9dcfc778-5fd6-4c68-8d37-a5385e374617	10
198861	sodium bicarbonate 650 MG Oral Tablet	SCD	9dcfc778-5fd6-4c68-8d37-a5385e374617	10
198861	NaHCO3 650 MG Oral Tablet	SY	9dcfc778-5fd6-4c68-8d37-a5385e374617	10
198861	sodium bicarbonate 10 Grains Oral Tablet	SY	9dcfc778-5fd6-4c68-8d37-a5385e374617	10
198861	sodium bicarbonate 648 MG Oral Tablet	SY	9dcfc778-5fd6-4c68-8d37-a5385e374617	10

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
69367-258-10	69367025810	1000 TABLET in 1 BOTTLE (69367-258-10)	1000 tablet	2022-10-10	0000-00-00	No	No	Current