DOSAGE & ADMINISTRATION SECTION
Directions:
Adult: Four tablets three times a day.
Ages below 12: half of the same or as prescribed by a homeopathic physician.
BM Sodium bicarbonate (Nat Bicarb)
- Manufacturer
- BM Private Limited
- Effective date
- 2025-12-02
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 02:35:36
Label at a glance#
ProductBM Sodium bicarbonate (Nat Bicarb)
Active ingredientSODIUM BICARBONATE
Label structure9 sections
Label contents#
Full prescribing information#
INACTIVE INGREDIENT SECTION
Inactive ingredients: Lactose; MAGNESIUM STEARATE
OTC - ACTIVE INGREDIENT SECTION
Sodium Bicarbonate
INDICATIONS & USAGE SECTION
Uses
See the leaflet enclosed for detail.
OTC - PURPOSE SECTION
Uses
See the leaflet enclosed for detail.
CONTRAINDICATIONS SECTION
Contra-indications:
Traditional biochemic remedy do not interact with other remedies, herbs, or other supplements.
WARNINGS SECTION
Warnings and Storage:
Ask a professional before use if pregnant or breastfeeding or if you have severe symptoms. Keep away from children. If you have a reaction to this product that is not positive, discontinue use. Store in a cool and dry place.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Warnings and Storage:
Ask a professional before use if pregnant or breastfeeding or if you have severe symptoms. Keep away from children. If you have a reaction to this product that is not positive, discontinue use. Store in a cool and dry place.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Data code | QR Code | BM Homoeopathic Pharmaceuticals Expanded cell salt Sodium bicarbonate 6X (Nat Bicarb 6X) Ref. standard: HPUS DRAP Mfg. Enl. # 0041, Prod. Enl. # 0041880721 NDC 82969-1036-1 | Sodium bicarbonate 6X.jpg |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 85816-1036-1 | BM Sodium bicarbonate (Nat Bicarb) | 30000 mg in 1 BOTTLE, GLASS | TABLET | 30000 | 2 |
Products#
Every source-derived product name is available through these pages.
- BM Sodium bicarbonate (Nat Bicarb)
- Sodium Bicarbonate
- SODIUM CATION
- MAGNESIUM STEARATE
- LACTOSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 85816-1036 | 85816-1036-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SODIUM BICARBONATE | 8MDF5V39QO | ACTIB |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| LACTOSE | J2B2A4N98G | IACT |
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 1 | 2025-06-20 | full-release | 2026-06-01 02:34:06 |
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 |
|---|---|---|---|---|---|---|
| BM Sodium bicarbonate (Nat Bicarb) | SODIUM BICARBONATE | BM Private Limited | 38044eae-7237-6add-e063-6294a90a827b | 2025-12-02 | Warnings | 85816-1036-1 85816-1036 85816103601 44fbb071-5ac8-c4f0-e063-6394a90a435e 38044eae-7237-6add-e063-6294a90a827b |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.