Indications and uses
relieves: acid indigestion heartburn sour stomach upset stomach associated with these symptoms
Sodium Bicarbonate Antacid - Rugby Laboratories
- Manufacturer
- Rugby Laboratories
- Effective date
- 2026-09-24
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 7
- Source
- daily-update
- Hydrated at
- 2026-09-26 01:01:53
Label at a glance#
ProductSodium Bicarbonate Antacid
Active ingredientSODIUM BICARBONATE
Label structure10 sections
Dosage and administration
do not use the maximum dosage for more than 2 weeks tablets may be swallowed whole or dissolved in water prior to use adults 60 years of age and over: 1-2 tablets every 4 hours, not more than 12 tablets in 24 hours adults under 60 years of age: 1-4 tablets every 4 hours, not more than 24 tablets in 24 hours
Contacts and useful links#
Websitewww.major-rugby.com
www.major-rugby.com
www.major-rugby.comWebsitewww.p65warnings.ca.gov
WWW.P65WARNINGS.CA.GOV
WWW.P65WARNINGS.CA.GOVLabel contents#
Full prescribing information#
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
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 the maximum dosage for more than 2 weeks, except under the advice and supervision of a physician.
OTC - ASK DOCTOR SECTION
Ask a doctor before use if you have a sodium restricted diet.
OTC - ASK DOCTOR/PHARMACIST SECTION
Ask a doctor or pharmacist before use if you are taking a prescription drug.
Antacids may interact with certain prescription drugs.
OTC - STOP USE SECTION
Stop use and ask a doctor if symptoms last more than 2 weeks
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast-feeding, ask a health professional before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children.
OVERDOSAGE SECTION
In case of accidental overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
Directions
- do not use the maximum dosage for more than 2 weeks
- tablets may be swallowed whole or dissolved in water prior to use
- adults 60 years of age and over: 1-2 tablets every 4 hours, not more than 12 tablets in 24 hours
- adults under 60 years of age: 1-4 tablets every 4 hours, not more than 24 tablets in 24 hours
Other information
- each tablet contains: sodium 178 mg
- store in a dry place at 15° – 30°C (59° – 86°F).
Inactive ingredients
croscarmellose sodium, microcrystalline cellulose, silica, stearic acid, talc.
Questions or comments?
1-800-231-4670
SPL UNCLASSIFIED SECTION
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.
Distributed by:
RUGBY® LABORATORIES
Indianapolis, IN 46268
(800) 616-2471
WARNING: THIS PRODUCT CAN EXPOSE YOU TO CHEMICALS INCLUDING LEAD AND MERCURY, WHICH ARE KNOWN TO THE STATE OF CALIFORNIA TO CAUSE BIRTH DEFECTS OR OTHER REPRODUCTIVE HARM. FOR MORE INFORMATION GO TO WWW.P65WARNINGS.CA.GOV.
Rev. 01/26 R-29 Re-order No. 370387
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Rugby®
NDC 0536-1047-10
sodium bicarbonate
sodium bicarbonate
10 gr (650 mg)
antacid
1000 tablets
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0305361047108 | GTIN-13: 0305361047108 EAN-13: 0305361047108 GTIN-12: 305361047108 UPC-A: 305361047108 GTIN storage (14 digits): 00305361047108 | 4624-1000G-Rugby-A2_LBL R54321.jpg |
DailyMed Product Concepts#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0536-1047-10 | EA - Each | 0536-1047 | fe82f6ce-ce8f-4ece-9ce3-f295a564ef98 | 1 | 2015-06-09 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| SODIUM BICARBONATE | ACTIVE INGREDIENT | 8MDF5V39QO | 2 | |
| SODIUM CATION | ACTIVE MOIETY | LYR4M0NH37 | 2 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | 2 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | 2 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | 2 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | 2 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | 2 |
Products#
Every source-derived product name is available through these pages.
- Sodium Bicarbonate Antacid
- Sodium Bicarbonate
- SODIUM CATION
- CROSCARMELLOSE SODIUM
- CELLULOSE, MICROCRYSTALLINE
- STEARIC ACID
- SILICON DIOXIDE
- TALC
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 0536-1047 | 0536-1047-10 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SODIUM BICARBONATE | 8MDF5V39QO | ACTIB |
| CROSCARMELLOSE SODIUM | M28OL1HH48 | IACT |
| CELLULOSE, MICROCRYSTALLINE | OP1R32D61U | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
| SILICON DIOXIDE | ETJ7Z6XBU4 | IACT |
| TALC | 7SEV7J4R1U | IACT |
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 6 | 2024-01-11 | full-release | 2026-06-01 00:07:00 |
Inactive ingredient matches#
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| SILICON DIOXIDE | SILICON DIOXIDE | ETJ7Z6XBU4 | TABLET / ORAL | 750 mg | ||
| STEARIC ACID | STEARIC ACID | 4ELV7Z65AP | TABLET / ORAL | 336 mg | ||
| TALC | TALC | 7SEV7J4R1U | TABLET / ORAL | 1000 mg | ||
| CROSCARMELLOSE SODIUM | CROSCARMELLOSE SODIUM | M28OL1HH48 | TABLET / ORAL | 736 mg | ||
| SILICON DIOXIDE | SILICON DIOXIDE | ETJ7Z6XBU4 | TABLET / ORAL | 750 mg | ||
| CELLULOSE, MICROCRYSTALLINE | MICROCRYSTALLINE CELLULOSE | OP1R32D61U | TABLET / ORAL | 6184 mg | ||
| STEARIC ACID | STEARIC ACID | 4ELV7Z65AP | TABLET / ORAL | 336 mg | ||
| CROSCARMELLOSE SODIUM | CROSCARMELLOSE SODIUM | M28OL1HH48 | TABLET / ORAL | 736 mg | ||
| CELLULOSE, MICROCRYSTALLINE | MICROCRYSTALLINE CELLULOSE | OP1R32D61U | TABLET / ORAL | 6184 mg | ||
| TALC | TALC | 7SEV7J4R1U | TABLET / ORAL | 1000 mg |
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 |
|---|---|---|---|---|---|---|
| 0eaf2d90-d844-3881-e063-6394a90a2742 | 28cdf049-acdb-4098-a5ca-e86257c81954 | 2024-01-11 | Warnings | 28cdf049-acdb-4098-a5ca-e86257c81954 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.