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 26 of 34 · 678 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Regular Strength Antacid Mint	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE	Topco Associates, LLC	59c16c09-c23d-4a37-8460-d6c00a268ed5	2024-12-26	Warnings	Exact identifier application number: M001
ANTACID	CALCIUM CARBONATE	Advance Pharmaceutical Inc.	face4e8c-3d0f-4c2e-83c1-44397b225ae7	2024-12-26	Warnings	Exact identifier application number: M001
ANTACID	CALCIUM CARBONATE	Advance Pharmaceutical Inc.	3203dfc5-2cb1-4703-8d81-63fba07ddd98	2024-12-26	Warnings	Exact identifier application number: M001
Magnesium Oxide	MAGNESIUM OXIDE	Richmond Pharmaceuticals, Inc.	9119b7f0-3e8a-7be7-e053-2995a90a4634	2024-12-26	Warnings	Exact identifier application number: M001
Magnesium Oxide	MAGNESIUM OXIDE	Richmond Pharmaceuticals, Inc.	db5941b2-0a04-452a-8fbc-bd5e40fadfb1	2024-12-26	Warnings	Exact identifier application number: M001
HEB Extra Strength Smooth Antacid Assorted Fruits	CALCIUM CARBONATE	H E B	2faac316-7b59-4df8-b751-37069e865263	2024-12-26	Warnings	Exact identifier application number: M001
Good Neighbor Pharmacy Antacid Extra Strength	CALCIUM CARBONATE	AmerisourceBergen Drug Corporation	5e3a3c20-dabe-4427-9e75-99759905caa0	2024-12-26	Warnings	Exact identifier application number: M001
Maximum Strength Antacid Cherry liquid	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE	Topco Associates, LLC	31d2e77d-5eda-4f47-917c-3390d6c782af	2024-12-26	Warnings	Exact identifier application number: M001
Maximum Strength Antacid Mint	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE	Topco Associates, LLC	50ceff1e-b6df-40f8-89f3-667cc8f9e750	2024-12-26	Warnings	Exact identifier application number: M001
HEB Extra Strength Smooth Antacid Peppermint	CALCIUM CARBONATE	H E B	d04e691e-6d1c-4c39-9504-7ac0f1bd197d	2024-12-26	Warnings	Exact identifier application number: M001
Antacid	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE	H E B	f294cf44-fb21-4b2e-8b7c-efd41416c6b2	2024-12-26	Warnings	Exact identifier application number: M001
Antacid	CALCIUM CARBONATE	Trifecta Pharmaceuticals USA LLC	14a7916e-5363-7f1b-e063-6294a90a20aa	2024-12-20	Warnings	Exact identifier application number: M001
maximum strength antacid cherry	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE	UNITED NATURAL FOODS, INC. DBA UNFI	d6b49f0a-cf05-4b1b-8cad-c5795aa31645	2024-12-20	Warnings	Exact identifier application number: M001
GOODSENSE Ultra Strength Antacid Peppermint	CALCIUM CARBONATE	GoodSense	04950b56-7760-4b6c-8110-86b6a3f795b4	2024-12-19	Warnings	Exact identifier application number: M001
Goodsense Regular Strength Antacid Peppermint	CALCIUM CARBONATE	GoodSense	32c04f3e-59f3-44aa-ad92-672444982710	2024-12-19	Warnings	Exact identifier application number: M001
GOODSENSE Ultra Strength Antacid Assorted Fruit	CALCIUM CARBONATE	GoodSense	ad4d51f6-b55b-45db-b034-fb3da54fbe99	2024-12-19	Warnings	Exact identifier application number: M001
TUMS Extra Strength Sugar-Free	CALCIUM CARBONATE	Haleon US Holdings LLC	3495102f-55d2-4a94-8d55-f46f49e00c27	2024-12-19	Warnings	Exact identifier application number: M001
Goodsense Extra Strength Antacid Assorted Fruit	CALCIUM CARBONATE	GoodSense	ae6270fc-0f8d-4bba-8f12-adba3f07f7c5	2024-12-19	Warnings	Exact identifier application number: M001
Quality Choice Extra Strength Assorted Berry Antacid Extra strength Assorted Berry Antacid	CALCIUM CARBONATE	Chain Drug Marketing Association Inc.	ec729051-72d3-4d1a-8e39-d4495d5c1cf3	2024-12-18	Warnings	Exact identifier application number: M001
Guardian Extra Strength Antacid	CALCIUM CARBONATE	Guardian Drug Company	aef3d830-c5c3-4f72-86ba-d31945a756db	2024-12-18	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