Indications and uses
For the relief of heartburn, sour stomach, acid indigestion, and upset stomach associated with these symptoms.
D&D SODIUM BICARBONATE
- Manufacturer
- Evi Labs
- Effective date
- 2026-01-14
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 01:33:43
Label at a glance#
ProductD-D SUDIUM BICARBONATE U.S.P. BICARBONATO DE SODA PURO
Active ingredientSODIUM BICARBONATE
Label structure13 sections
Dosage and administration
Adults and children 12 years of age and over: Mix 1/4 teaspoonful in water and drink. Do not use more than 4 times a day. For children under 12 years of age, ask a doctor.
Label contents#
Full prescribing information#
Active Ingredients
Sodium Bicarbonate U.S.P. 100%
Purpose
Antacid
Uses
For the relief of heartburn, sour stomach, acid indigestion, and upset stomach associated with these symptoms.
Warnings
Do not exceed the maximum daily dosage. Do not take more than four 1/4 teaspoonfuls in 24 hours. Do not use the maximum dosage of this product for more than 2 weeks.
Do not use if you are on a sodium-restricted diet.
If pregnant or breastfeeding, ask a health professional before use.
Keep out of reach of children
In case of overdose, get medical help or contact aPoison Control Center right away
Directions
Adults and children 12 years of age and over: Mix 1/4 teaspoonful in water and drink.
Do not use more than 4 times a day. For children under 12 years of age, ask a doctor.
Other Information
Store at controlled room temperature 15º-25ºC (59º-86ºF). This package is old by weight, ot volume. Some settings of contents may have occurred during shipping and handling.
Inactive ingredients
none
Tamper-Evident Disclosure
Do not use if the printed over-wrap over the bottle cap is torn, broken, or missing.
Principal Display Panel
Package Label 4 oz
Package Label 8 oz
Package Label 16 oz
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| BICARBONATE ION Pharmacologic Class Indexing | 1 | Indexing - Pharmacologic Class | 20220121 |
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0748541492167 | GTIN-13: 0748541492167 EAN-13: 0748541492167 GTIN-12: 748541492167 UPC-A: 748541492167 GTIN storage (14 digits): 00748541492167 | D - D Sodium Bicarbonate 16 Oz.jpg |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 84178-105-02 | D-D SUDIUM BICARBONATE U.S.P.BICARBONATO DE SODA PURO | 113 g in 1 BOTTLE, PLASTIC | POWDER | 113 | 1 | |
| 84178-105-03 | D-D SUDIUM BICARBONATE U.S.P.BICARBONATO DE SODA PURO | 227 g in 1 BOTTLE, PLASTIC | POWDER | 227 | 1 | |
| 84178-105-04 | D-D SUDIUM BICARBONATE U.S.P.BICARBONATO DE SODA PURO | 454 g in 1 BOTTLE, PLASTIC | POWDER | 454 | 1 |
Products#
Every source-derived product name is available through these pages.
- D-D SUDIUM BICARBONATE U.S.P. BICARBONATO DE SODA PURO
- SODIUM BICARBONATE
- SODIUM CATION
- BICARBONATE ION
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 84178-105 | 84178-105-02, 84178-105-03, 84178-105-04 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SODIUM BICARBONATE | 8MDF5V39QO | ACTIB |
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 |
|---|---|---|---|---|---|---|
| D-D SUDIUM BICARBONATE U.S.P. BICARBONATO DE SODA PURO | SODIUM BICARBONATE | Evi Labs | 485f9eb1-6535-c47c-e063-6394a90ae32c | 2026-01-14 | Warnings | 84178-105-04 84178-105-02 84178-105-03 84178-105 84178010503 84178010502 84178010504 485f9eb1-6536-c47c-e063-6394a90ae32c 485f9eb1-6535-c47c-e063-6394a90ae32c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.