Sodium Bicarbonate 5 gr

Product NDC: 55681-307
11-digit product format: 556810307
Labeler code: 55681
Product ID: 55681-307_583275fa-14ea-1816-e063-6394a90a48f9
Type: HUMAN OTC DRUG
Nonproprietary name: Sodium Bicarbonate
Dosage form: TABLET
Route: ORAL
Labeler: TWIN MED LLC
Application: M001
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2022-06-30
Marketing end: 2029-12-31
Substance: SODIUM BICARBONATE
Active strength: 325 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
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 5 gr

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SODIUM BICARBONATE	325 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
198859	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
e325d899-d9a6-5adb-e053-2995a90ac861	Available on FDA.report

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
55681-307-02	Sodium Bicarbonate 5 gr	200 in 1 BOTTLE	TABLET	200		7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55681-307	SODIUM BICARBONATE 5 GR (SODIUM BICARBONATE) TABLET [TWIN MED LLC]	6	Current NDC, Legacy NDC, 1 package rows	20250425_e325d899-d9a6-5adb-e053-2995a90ac861.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 20 of 34 · 678 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Leader Ultra Strength Antacid	CALCIUM CARBONATE	CARDINAL HEALTH 110, LLC. DBA LEADER	eab5a905-67fb-494e-8f55-aeeab4c2dce2	2025-08-22	Warnings	Exact identifier application number: M001
Leader Extra Strength Antacid	CALCIUM CARBONATE	CARDINAL HEALTH 110, LLC. DBA LEADER	81911f6d-7edf-4183-9720-2f20a5db498d	2025-08-21	Warnings	Exact identifier application number: M001
Gas Relief	SIMETHICONE	BJWC (Berkley & Jensen / BJ's)	2f32dde8-502e-eefa-e063-6294a90abf20	2025-08-19	Warnings	Exact identifier application number: M001
CVS Health Ultra Strength Natural Antacid Peppermint Flavor	ANTACID TABLETS	CVS Pharmacy,Inc.	4f18fd8d-4d6a-4b1d-8a94-b64592f73ad0	2025-08-13	Warnings	Exact identifier application number: M001
MGC Health Calcium Carbonate Antacid Assorted Berries	CALCIUM CARBONATE	Xiamen Kang Zhongyuan Biotechnology Co., Ltd.	b84d80c6-0240-4276-8e47-74a918f3d86a	2025-08-12	Warnings	Exact identifier application number: M001
Antacid	CALCIUM CARBONATE	ProStat First Aid	3bb49eb3-2eaa-af8d-e063-6294a90a4035	2025-08-06	Warnings	Exact identifier application number: M001
Maximum Strength Antacid and Antigas	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE	Meijer, Inc.	30a0455d-63e0-95cc-e063-6394a90ada6b	2025-07-30	Warnings	Exact identifier application number: M001
Sodium Bicarbonate Antacid	SODIUM BICARBONATE	Menper Distributors Inc.	6efb4da0-03ae-4df6-acd7-e8023d20d4b3	2025-07-22	Warnings	Exact identifier application number: M001
Gas-X Total Relief Maximum Strength	CALCIUM CARBONATE, SIMETHICONE	Haleon US Holdings LLC	edb0f11a-bdb7-484d-9257-09ff47b0fca4	2025-07-15	Warnings	Exact identifier application number: M001
REGULAR STRENGTH ANTACID ANTIGAS	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE	WALGREEN COMPANY	7cd9234e-d1cc-4cce-e053-2991aa0a457e	2025-07-09	Warnings	Exact identifier application number: M001
Sodium Bicarbonate	SODIUM BICARBONATE	Westminster Pharmaceuticals, LLC	9dcfc778-5fd6-4c68-8d37-a5385e374617	2025-07-08	Warnings	Exact identifier application number: M001
MGC Health Antacid Soft Chews Cherry Flavor	CALCIUM CARBONATE	Xiamen Kang Zhongyuan Biotechnology Co., Ltd.	3958ec0a-8f32-6918-e063-6294a90ac1c4	2025-07-07	Warnings	Exact identifier application number: M001
Aluminum Hydroxide, Magnesium Hydroxide, and Simethicone	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, AND SIMETHICONE	Major Pharmaceuticals	1bc90fa7-fcce-4a9b-862f-f30ab602ecab	2025-07-07	Warnings	Exact identifier application number: M001
KOSHER MEDS antacid	CALCIUM CARBONATE	Mollec Inc	7783d6a2-56e3-4542-ad1d-60680e03532b	2025-07-01	Warnings	Exact identifier application number: M001
Nauzene Chewables Ginger Honey	SODIUM CITRATE	Kobayashi Healthcare International, Inc.	25c9825d-a4e8-4671-e063-6294a90ab46d	2025-06-24	Warnings	Exact identifier application number: M001
Gaviscon Extra Strength	ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE	Haleon US Holdings LLC	7f367927-c366-465c-a059-e2cfb337d562	2025-06-11	Warnings	Exact identifier application number: M001
Calmicid AC Acid Reducer	FAMOTIDINE	Melaleuca, Inc.	369ae213-cd23-57ba-e063-6394a90a87a6	2025-06-02	Warnings	Exact identifier application number: M001
Aluminum Hydroxide, Magnesium Hydroxide, and Simethicone	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, AND SIMETHICONE	American Health Packaging	2faf291e-1d62-412a-a05e-e992cb7def6a	2025-05-30	Warnings	Exact identifier application number: M001
Kids Tummy Relief	CALCIUM CARBONATE	Genexa Inc.	a7831b84-1f51-9258-e053-2a95a90a901e	2025-05-23	Warnings	Exact identifier application number: M001
Calcium Carbonate	CALCIUM CARBONATE	Atlantic Biologicals Corps	38654d22-2f8a-49d2-a1cd-06d341f11323	2025-05-12	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
198859	sodium bicarbonate 325 MG Oral Tablet	PSN	e325d899-d9a6-5adb-e053-2995a90ac861	7
198859	sodium bicarbonate 325 MG Oral Tablet	SCD	e325d899-d9a6-5adb-e053-2995a90ac861	7
198859	NaHCO3 325 MG Oral Tablet	SY	e325d899-d9a6-5adb-e053-2995a90ac861	7
198859	sodium bicarbonate 324 MG Oral Tablet	SY	e325d899-d9a6-5adb-e053-2995a90ac861	7
198859	sodium bicarbonate 5 Grains Oral Tablet	SY	e325d899-d9a6-5adb-e053-2995a90ac861	7

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
55681-307-02	55681030702	200 TABLET in 1 BOTTLE (55681-307-02)	200 tablet	2022-06-30	2029-12-31	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Twin Med - Sodium Bicarbonate 5 gr, 325 mg (55681-307)	TWIN MED LLC \| ELYSIUM PHARMACEUTICALS LIMITED	2026-08-04	HUMAN OTC DRUG LABEL	8