Sodium Bicarbonate

Product NDC: 0904-7261
11-digit product format: 009047261
Labeler code: 0904
Product ID: 0904-7261_5c3c65f4-91c6-1cca-e063-6394a90ae62f
Type: HUMAN OTC DRUG
Nonproprietary name: Sodium Bicarbonate
Dosage form: TABLET
Route: ORAL
Labeler: Major Pharmaceuticals
Application: M001
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2022-10-26
Substance: SODIUM BICARBONATE
Active strength: 650 mg/1
Pharmacologic classes: Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
NDC exclude flag: No
Listing certified through: 2027-12-31
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: 2027-12-31

Active Ingredients#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
95250459-30e4-45c1-b08a-993044f49109	Product name	2	20250805
726062af-1135-4707-a1d7-57256991bbf9	Product name	2	20250226
a21a21e5-f36d-4c1f-8918-def921b8f7e3	Product name	3	20250124
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
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7	Product name	2	20211025
9badc7be-250a-44ab-aa36-926af3f02679	Product name	1	20210527
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	5	20200925
e4870509-7e28-6f92-f0be-dd3dd889a9cf	Product name	5	20200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cd	Product name	2	20190619
444b3e50-f226-46ef-bfca-2e7035d140cd	Product name	1	20190611
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
26acd337-b838-40ac-bcbc-05c3b81c8712	Product name	1	20170323
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	2	20160823
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
290f523a-f9db-9774-b5a9-e1f908ac1782	Product name	1	20150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316
19c71a3d-ed9c-166b-a7e5-38c250c35631	Product name	1	20140508
5668b646-cd56-c3c7-bdea-3f6b1a8840db	Product name	1	20140508
597b1cfd-7b31-5048-62be-ca5cd740da2f	Product name	1	20140508
684ea482-2e8b-14af-5664-b98f1e402036	Product name	1	20140508
810ab97e-f109-f41c-7c83-6a652a9cbf43	Product name	1	20140508
87711080-88eb-65c5-b2dd-bf99e700a372	Product name	1	20140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2dd	Product name	1	20140508
b060cc1a-fe47-856b-0b77-4448b5963de8	Product name	1	20140508
c6b65c52-69c7-df49-550a-a50c137f6218	Product name	1	20140508
ec2149b3-5c6d-5344-f757-c86411073075	Product name	1	20140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0904-7261-61	Sodium Bicarbonate	10 in 1 BOX, UNIT-DOSE	TABLET	10		2
0904-7261-61	Sodium Bicarbonate	10 in 1 BLISTER PACK	TABLET	10		2

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0904-7261-61	EA - Each	0904-7261	12c9d63e-c7b6-4a45-b31d-ec8a7bcd7e18	1	2022-12-07

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0904-7261	SODIUM BICARBONATE TABLET [MAJOR PHARMACEUTICALS]	2	Current NDC, Legacy NDC, 2 package rows	20241208_ebf340c9-0b6d-13d2-e053-2995a90ae338.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 15 of 34 · 678 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
SUPREME ANTACID	CALCIUM CARBONATE, MAGNESIUM HYDROXIDE	FAMILY DOLLAR SERVICES INC	5e996df3-25a4-b259-e053-2a91aa0a4311	2025-11-19	Warnings	Exact identifier application number: M001
GERI-LANTA ANTACID ANTIGAS	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	Geri-Care Pharmaceuticals, Corp	a7d7298f-44d6-4e09-8578-7fe311243002	2025-11-19	Warnings	Exact identifier application number: M001
GERI-MOX MAX CHERRY	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	Geri-Care Pharmaceuticals, Corp	8e57bcf5-2960-4c41-8bf2-83cb1ee50168	2025-11-19	Warnings	Exact identifier application number: M001
Tums Antacid Chewy Bites	CALCIUM CARBONATE 750 MG	R J General Corporation	6208d11d-0670-4a20-a3fc-ebc764a8e6cd	2025-11-17	Warnings	Exact identifier application number: M001
REGULAR STRENGTH ANTACID/ANTIGAS	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	RUGBY LABORATORIES	b244fce9-9626-e947-e053-2995a90ab8f9	2025-11-17	Warnings	Exact identifier application number: M001
Antacid Childrens	CALCIUM CARBONATE	CVS Pharmacy	08953df1-cc29-452f-bc69-b19970a1fd2e	2025-11-15	Warnings	Exact identifier application number: M001
Magnesium Oxide	MAGNESIUM OXIDE	Marlex Pharmaceuticals Inc	0bb322a5-fb92-14de-e063-6294a90a4c1b	2025-11-14	Warnings	Exact identifier application number: M001
magnesium oxide	MAGNESIUM OXIDE	Marlex Pharmaceuticals Inc.	dc57893c-068a-37d8-e053-2a95a90aa054	2025-11-14	Warnings	Exact identifier application number: M001
Earthmed Soothe Chewable Orange	CITRIC ACID	Earthmed LLC	439543fe-ceb9-4c5c-e063-6294a90a9b70	2025-11-14	Warnings	Exact identifier application number: M001
MAXIMUM STRENGTH ANTACID MINT	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	CVS	3ce054f3-2953-5f7d-e054-00144ff8d46c	2025-11-11	Warnings	Exact identifier application number: M001
Topcare Antacid Extra Strength Assorted Berry	CALCIUM CARBONATE	Topco Associates LLC	14f6f475-32d6-4783-8dcc-1fe265902d55	2025-11-10	Warnings	Exact identifier application number: M001
Topcare Antacid Calcium	CALCIUM CARBONATE	Topco Associates LLC	38c26f49-fb5e-480c-9164-bf5edcf0726b	2025-11-10	Warnings	Exact identifier application number: M001
Topcare Antacid Calcium	CALCIUM CARBONATE	Topco Associates LLC.	bb99b942-1f84-43e1-a18d-3a975cddc59e	2025-11-08	Warnings	Exact identifier application number: M001
Topcare Antacid Calcium Regular Strength	CALCIUM CARBONATE	Topco Associates LLC	2606ac08-9760-4ff6-8d90-51fbb04e6ac8	2025-11-08	Warnings	Exact identifier application number: M001
Topcare Antacid Calcium Extra Strength	CALCIUM CARBONATE	Topco Associates LLC	495d97b0-d95c-46d1-a76a-56ac7f823538	2025-11-08	Warnings	Exact identifier application number: M001
Topcare Antacid Calcium Extra Strength	CALCIUM CARBONATE	Topco Associates LLC.	73b4cda2-900a-4380-a0ae-0abfecdb7263	2025-11-08	Warnings	Exact identifier application number: M001
Topcare Extra Strength Antacid Assorted Fruit	CALCIUM CARBONATE	Topco Associates LLC	2677ca2b-b211-475e-a9c4-643fd54a744f	2025-11-08	Warnings	Exact identifier application number: M001
TopCare Antacid Calcium	CALCIUM CARBONATE	Topco Associates LLC	b94eac38-62d0-49a2-bb49-053fda8129e2	2025-11-08	Warnings	Exact identifier application number: M001
Topcare Antacid Calcium	CALCIUM CARBONATE	Topco Associates LLC	04b3d397-df99-44e2-a191-6e9199b08398	2025-11-08	Warnings	Exact identifier application number: M001
topcare Antacid Calcium Ultra Strength	CALCIUM CARBONATE	Topco Associates LLC	6e2788b3-1e33-4908-aa2c-475d69b94ee6	2025-11-08	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	60c2a176-8854-4479-b853-d07fe9a1830c	4
198861	sodium bicarbonate 650 MG Oral Tablet	SCD	60c2a176-8854-4479-b853-d07fe9a1830c	4
198861	NaHCO3 650 MG Oral Tablet	SY	60c2a176-8854-4479-b853-d07fe9a1830c	4
198861	sodium bicarbonate 10 Grains Oral Tablet	SY	60c2a176-8854-4479-b853-d07fe9a1830c	4
198861	sodium bicarbonate 648 MG Oral Tablet	SY	60c2a176-8854-4479-b853-d07fe9a1830c	4
198861	sodium bicarbonate 650 MG Oral Tablet	PSN	ebf340c9-0b6d-13d2-e053-2995a90ae338	2
198861	sodium bicarbonate 650 MG Oral Tablet	SCD	ebf340c9-0b6d-13d2-e053-2995a90ae338	2
198861	NaHCO3 650 MG Oral Tablet	SY	ebf340c9-0b6d-13d2-e053-2995a90ae338	2
198861	sodium bicarbonate 10 Grains Oral Tablet	SY	ebf340c9-0b6d-13d2-e053-2995a90ae338	2
198861	sodium bicarbonate 648 MG Oral Tablet	SY	ebf340c9-0b6d-13d2-e053-2995a90ae338	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0904-7261-61	00904726161	10 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-7261-61) / 10 TABLET in 1 BLISTER PACK	10 blister pack	2022-10-26	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
4624 - Major	Major Pharmaceuticals	2026-09-24	HUMAN OTC DRUG LABEL	3
Sodium Bicarbonate	Cardinal Health 107, LLC	2026-06-12	HUMAN OTC DRUG LABEL	5