Sodium Bicarbonate 10 gr
- Product NDC
- 69618-034
- 11-digit product format
- 696180034
- Labeler code
- 69618
- Product ID
- 69618-034_2bc8028b-eebb-902f-e063-6394a90a382b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Bicarbonate
- Dosage form
- TABLET, SOLUBLE
- Route
- ORAL
- Labeler
- Reliable 1 Laboratories LLC
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2015-11-01
- Substance
- SODIUM BICARBONATE
- Active strength
- 648 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
- 2026-12-31
- Current FDA listing
- Yes
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Package NDC | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|
| 2024-11-09 02:27 UTC · source 2024-11-08 | excluded product | product | ad56d346431e… | cc804d4bbf1e… | |
| 2024-11-09 02:27 UTC · source 2024-11-08 | excluded package | package | 69618-034-10 | ad56d346431e… | cc804d4bbf1e… |
| 2024-10-04 04:10 UTC · source 2024-10-03 | excluded product | product | 367a005e9d99… | 383a685ebd0f… | |
| 2024-10-04 04:10 UTC · source 2024-10-03 | excluded package | package | 69618-034-10 | 367a005e9d99… | 383a685ebd0f… |
| 2024-07-10 04:00 UTC · source 2024-07-09 | excluded product | product | 557ba5c1ecfa… | 9c80585c8c6e… | |
| 2024-07-10 04:00 UTC · source 2024-07-09 | excluded package | package | 69618-034-10 | 557ba5c1ecfa… | 9c80585c8c6e… |
| 2024-05-28 21:12 UTC · source 2024-05-28 | excluded product | product | 8af77b9d5b6f… | d9bbb34c5368… | |
| 2024-05-28 21:12 UTC · source 2024-05-28 | excluded package | package | 69618-034-10 | 8af77b9d5b6f… | d9bbb34c5368… |
| 2024-05-15 03:39 UTC · source 2024-05-14 | excluded product | product | 834df4deac94… | adcc014656a3… | |
| 2024-05-15 03:39 UTC · source 2024-05-14 | excluded package | package | 69618-034-10 | 834df4deac94… | adcc014656a3… |
| 2024-03-11 06:39 UTC · source 2024-03-08 | excluded product | product | 1332a3947898… | d4bfe170f9cd… | |
| 2024-03-11 06:39 UTC · source 2024-03-08 | excluded package | package | 69618-034-10 | 1332a3947898… | d4bfe170f9cd… |
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 10 gr
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| SODIUM BICARBONATE | 648 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 8MDF5V39QO | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 198861 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 321a772c-c44c-3d4e-e054-00144ff8d46c | Available on FDA.report |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 69618-034-10 | 2023-01-30 | C162847 | 48780-1 | f386c64a-1db3-0266-e053-dadaa90a7c1a | Sodium Bicarbonate 10 gr |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69618-034-10 | Sodium Bicarbonate 10 gr | 1000 in 1 BOTTLE, PLASTIC | TABLET, SOLUBLE | 1000 | 6 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 69618-034-10 | EA - Each | 69618-034 | 8774e945-56f9-47f5-8fab-22387140da43 | 1 | 2016-05-16 |
DailyMed Dashboard NDC Coverage#
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 |
|---|---|---|---|---|---|---|
| cherry antacid soft chew | CALCIUM CARBONATE | American Sales | 49261864-e596-20e5-e054-00144ff8d46c | 2025-12-07 | Warnings | M001 |
| Assorted Fruit Antacid Flavor Chews | CALCIUM CARBONATE | CVS Pharmacy | 3c679059-2532-485a-e054-00144ff88e88 | 2025-12-07 | Warnings | M001 |
| Antacid Fruit Chews | CALCIUM CARBONATE | CVS Pharmacy | 4a527608-b4d4-57c0-e054-00144ff88e88 | 2025-12-07 | Warnings | M001 |
| Heartburn and gas fruit chews | CALCIUM CARBONATE | CVS Pharmacy | 4a656a9f-8f34-69b7-e054-00144ff8d46c | 2025-12-07 | Warnings | M001 |
| Orange Antacid Soft Chew | CALCIUM CARBONATE | CVS Pharmacy | 4a67f0d0-788b-433b-e054-00144ff88e88 | 2025-12-07 | Warnings | M001 |
| Cherry Antacid Soft Chews | CALCIUM CARBONATE | CVS Pharmacy | 61e4e83c-ee98-579d-e053-2991aa0ab099 | 2025-12-07 | Warnings | M001 |
| CVS Mixed Berry Antacid HBG 54ct | CALCIUM CARBONATE | CVS Pharmacy | e9204edb-e4d9-3975-e053-2995a90ac6a9 | 2025-12-07 | Warnings | M001 |
| CVS Mixed Berry Antacid HBG 28ct | CALCIUM CARBONATE | CVS Pharmacy | e9481d36-3b28-5caf-e053-2a95a90a3121 | 2025-12-07 | Warnings | M001 |
| CVS Wild Berry Antacid Chews | CALCIUM CARBONATE | CVS Pharmacy | f6f45d9c-f9fc-225b-e053-6394a90a30e1 | 2025-12-07 | Warnings | M001 |
| CVS Wild Berry Antacid Chews | CALCIUM CARBONATE | CVS Pharmacy | f6f5dc9a-b573-70c1-e053-6394a90acdb0 | 2025-12-07 | Warnings | M001 |
| Basic Care Antacid Fruit Chews | CALCIUM CARBONATE | Amazon.com | c8d2b8aa-fce4-f973-e053-2995a90a6edd | 2025-12-05 | Warnings | M001 |
| Basic Care Berry Antacid HBG | CALCIUM CARBONATE | Amazon.com | c8d4050e-75fd-2445-e053-2995a90a7b0d | 2025-12-05 | Warnings | M001 |
| QUALITY CHOICE Regular Strength | ANTACID TABLETS (CALCIUM CARBONATE) | QUALITY CHOICE (Chain drug Marketing Assoiciation) | fce6c50d-908f-44a6-ba63-ece813f3711b | 2025-12-04 | Warnings | M001 |
| QUALITY CHOICE Regular Strength | ANTACID TABLETS (CALCIUM CARBONATE) | QUALITY CHOICE (Chain drug Marketing Assoiciation) | 667ffb59-9bff-45a7-89f0-ccfa0d841909 | 2025-12-04 | Warnings | M001 |
| QUALITY CHOICE | CALCIUM CARBONATE | QUALITY CHOICE (Chain drug Marketing Assoiciation) | 9ff282fd-7623-4c9e-8faa-c51e33a7616e | 2025-12-04 | Warnings | M001 |
| QUALITY CHOICE Extra Strength | ANTACID TABLETS (CALCIUM CARBONATE) | QUALITY CHOICE (Chain drug Marketing Assoiciation) | 7c948dc6-e569-46d2-8edd-59da48857e0e | 2025-12-04 | Warnings | M001 |
| QUALITY CHOICE Ultra Strength | ANTACID TABLETS (CALCIUM CARBONATE) | QUALITY CHOICE (Chain drug Marketing Assoiciation) | b074a885-5d10-46e4-8de9-dd9460968dad | 2025-12-04 | Warnings | M001 |
| Quality Choice Extra Strength | ANTACID TABLETS (CALCIUM CARBONATE) | QUALITY CHOICE (Chain drug Marketing Assoiciation) | 2bb8ccb6-6275-4ace-8096-ee545501df39 | 2025-12-04 | Warnings | M001 |
| Quality Choice Ultra Strength | ANTACID TABLET (CALCIUM CARBONATE) | QUALITY CHOICE (Chain drug Marketing Assoiciation) | cdac56f1-e579-4943-a24a-6564c30086d2 | 2025-12-04 | Warnings | M001 |
| QUALITY CHOICE Original Flavor | ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE | CHAIN DRUG MARKETING ASSOCIATION INC. | a699b830-6400-4af9-9810-5eda79157333 | 2025-12-04 | Warnings | M001 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 198861 | sodium bicarbonate 650 MG Oral Tablet | PSN | 321a772c-c44c-3d4e-e054-00144ff8d46c | 6 |
| 198861 | sodium bicarbonate 650 MG Oral Tablet | SCD | 321a772c-c44c-3d4e-e054-00144ff8d46c | 6 |
| 198861 | NaHCO3 650 MG Oral Tablet | SY | 321a772c-c44c-3d4e-e054-00144ff8d46c | 6 |
| 198861 | sodium bicarbonate 10 Grains Oral Tablet | SY | 321a772c-c44c-3d4e-e054-00144ff8d46c | 6 |
| 198861 | sodium bicarbonate 648 MG Oral Tablet | SY | 321a772c-c44c-3d4e-e054-00144ff8d46c | 6 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 69618-034-10 | 69618003410 | 1000 TABLET, SOLUBLE in 1 BOTTLE, PLASTIC (69618-034-10) | 2015-11-01 | 0000-00-00 | No | No | Current |