Indications and uses
relieves acid indigestion heartburn sour stomach upset stomach associated with these symptoms
Sodium Bicarbonate
- Manufacturer
- Westminster Pharmaceuticals, LLC
- Effective date
- 2025-07-08
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 10
- Source
- full-release
- Hydrated at
- 2026-06-01 01:06:49
Label at a glance#
ProductSodium Bicarbonate
Active ingredientSODIUM BICARBONATE
Label structure10 sections
Dosage and administration
Take 1 tablet, dissolved in a glass of water, as needed. Maximum daily dose for adults up to 60 years of age is 24 tablets. Maximum daily dose for adults 60 years of age or older is 12 tablets. Dissolve completely in water before drinking. DO NOT EXCEED RECOMMENDED DOSE. Not recommended for children.
Storage and handling
each tablet contains: sodium 178 mg (7.74 mEq) store at room temperature 15º-30ºC (59º-86°F) in a well-closed container as defined in the USP
Contacts and useful links#
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
Active ingredient (in each tablet)
Sodium Bicarbonate 10 gr (650 mg)
Purpose
Antacid
Uses
relieves
- acid indigestion
- heartburn
- sour stomach
- upset stomach associated with these symptoms
Warnings
OTC - DO NOT USE SECTION
Do not use this product if you are on a sodium-restricted diet unless directed by a doctor. Do not take more than 24 tablets for adults up to 60 years of age (or 12 tablets for adults 60 years of age and older) in a 24 hour period nor use maximum dosage for more than 2 weeks, except under the advice and supervision of a physician. As with any drug, if you are pregnant or nursing a baby, seek advice of a health professional before using this product.
Stomach Warning
TO AVOID SERIOUS INJURY, DO NOT TAKE UNTIL TABLET IS COMPLETELY DISSOLVED IT IS VERY IMPORTANT NOT TO TAKE THIS PRODUCT WHEN OVERLY FULL FROM FOOD OR DRINK.
Consult a doctor if severe stomach pain occurs after taking this product.
Drug Interaction Precaution
Ask a physician or pharmacist before use if you are presently taking a prescription drug. Antacids may interact with certain prescription drugs.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
KEEP THIS AND ALL DRUGS OUT OF THE REACH OF CHILDREN. In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately.
Directions
Adults
Take 1 tablet, dissolved in a glass of water, as needed. Maximum daily dose for adults up to 60 years of age is 24 tablets. Maximum daily dose for adults 60 years of age or older is 12 tablets. Dissolve completely in water before drinking.
DO NOT EXCEED RECOMMENDED DOSE. Not recommended for children.
Other information
- each tablet contains: sodium 178 mg (7.74 mEq)
- store at room temperature 15º-30ºC (59º-86°F) in a well-closed container as defined in the USP
Inactive ingredients
Microcrystalline cellulose and stearic acid
Questions or comments?
Call 1-844-221-7294 M-F (9 a.m. to 5 p.m. EST)
PRINCIPAL DISPLAY PANEL - 1000 Tablet Bottle Label
NDC 69367-258-10
Sodium Bicarbonate
Tablets, USP
10 gr (650 mg)
ANTACID
THIS PACKAGE FOR HOUSEHOLDS
WITHOUT YOUNG CHILDREN.
1000 Tablets
WP
Westminster
Pharmaceuticals
DailyMed RxNorm Mappings#
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| BICARBONATE ION Pharmacologic Class Indexing | 1 | Indexing - Pharmacologic Class | 20220121 |
DailyMed Product Concepts#
| 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 | 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 | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 69367-258-10 | EA - Each | 69367-258 | a1b249a4-e5e5-4321-8168-8cc6532ba91d | 1 | 2022-11-07 |
Products#
Every source-derived product name is available through these pages.
- Sodium Bicarbonate
- BICARBONATE ION
- MICROCRYSTALLINE CELLULOSE
- STEARIC ACID
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 69367-258 | 69367-258-10 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SODIUM BICARBONATE | 8MDF5V39QO | ACTIB |
| MICROCRYSTALLINE CELLULOSE | OP1R32D61U | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Sodium Bicarbonate | SODIUM BICARBONATE | Westminster Pharmaceuticals, LLC | 9dcfc778-5fd6-4c68-8d37-a5385e374617 | 2025-07-08 | Warnings | 69367-258-10 69367-258 69367025810 43b42880-bab8-4580-8a00-ae13855d44a3 9dcfc778-5fd6-4c68-8d37-a5385e374617 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.