Sodium Bicarbonate 10 gr. (650 mg)
- Product NDC
- 77333-829
- 11-digit product format
- 773330829
- Labeler code
- 77333
- Product ID
- 77333-829_4f52483b-6426-9646-e063-6394a90a5c0b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Bicarbonate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Gendose Pharmaceuticals, LLC
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-05-01
- Substance
- SODIUM BICARBONATE
- Active strength
- 650 mg/1
- Pharmacologic classes
- Alkalinizing Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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 10 gr. (650 mg)
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| SODIUM BICARBONATE | 650 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 |
|---|---|
| 0a0cc46d-372e-4175-932a-065e82d8d353 | Available on FDA.report |
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 |
|---|---|---|---|---|---|---|
| 77333-829-10 | Sodium Bicarbonate 10 gr. (650 mg) | 100 in 1 BOX, UNIT-DOSE | TABLET | 100 | 1 | |
| 77333-829-25 | Sodium Bicarbonate 10 gr. (650 mg) | 10 in 1 BLISTER PACK | TABLET | 10 | 1 |
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 |
|---|---|---|---|---|---|---|
| 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 |
| Alka-Seltzer Heartburn Relief Peppermint | CALCIUM CARBONATE | Bayer HealthCare LLC. | 9b8e802f-91b6-4559-e053-2a95a90aff67 | 2025-12-04 | Warnings | M001 |
| Alka-Seltzer Cool Action Heartburn Relief Mint | CALCIUM CARBONATE | Bayer HealthCare LLC. | 9b8da147-8d0c-e6b0-e053-2a95a90a35e6 | 2025-12-04 | Warnings | M001 |
| Alka-Seltzer Kids Tummy ReliefChews | CALCIUM CARBONATE AND DIMETHICONE | Bayer HealthCare LLC. | ba48966e-3762-5fdf-e053-2995a90aeb3d | 2025-12-04 | Warnings | M001 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 198861 | sodium bicarbonate 650 MG Oral Tablet | PSN | 0a0cc46d-372e-4175-932a-065e82d8d353 | 1 |
| 198861 | sodium bicarbonate 650 MG Oral Tablet | SCD | 0a0cc46d-372e-4175-932a-065e82d8d353 | 1 |
| 198861 | NaHCO3 650 MG Oral Tablet | SY | 0a0cc46d-372e-4175-932a-065e82d8d353 | 1 |
| 198861 | sodium bicarbonate 10 Grains Oral Tablet | SY | 0a0cc46d-372e-4175-932a-065e82d8d353 | 1 |
| 198861 | sodium bicarbonate 648 MG Oral Tablet | SY | 0a0cc46d-372e-4175-932a-065e82d8d353 | 1 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 77333-829-10 | 77333082910 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (77333-829-10) / 10 TABLET in 1 BLISTER PACK (77333-829-25) | 100 blister pack | 2026-05-01 | No | No | Current |
| 77333-829-25 | 77333082925 | 10 in 1 BLISTER PACK | Historical |