BM Sodium bicarbonate (Nat Bicarb)
- Product NDC
- 85816-1036
- 11-digit product format
- 858161036
- Labeler code
- 85816
- Product ID
- 85816-1036_44fbb071-5ac8-c4f0-e063-6394a90a435e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Bicarbonate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- BM Private Limited
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2025-06-01
- Substance
- SODIUM BICARBONATE
- Active strength
- 6 [hp_X]/60mg
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BM Sodium bicarbonate (Nat Bicarb)
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM BICARBONATE | 6 [hp_X]/60mg |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8MDF5V39QO |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| 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 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85816-1036-1 | 85816103601 | 30000 mg in 1 BOTTLE, GLASS (85816-1036-1) | 30000 mg | 2025-06-01 | No | No | Historical |