KALI SULPHURICUM
- Product NDC
- 76472-4094
- 11-digit product format
- 764724094
- Labeler code
- 76472
- Product ID
- 76472-4094_2ddc53bf-0bf5-fb07-e063-6394a90aa1cd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- KALI SULPHURICUM
- Dosage form
- PELLET
- Route
- SUBLINGUAL
- Labeler
- SEVENE USA
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2023-06-26
- Substance
- POTASSIUM SULFATE
- Active strength
- 6 [hp_X]/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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- KALI SULPHURICUM
- Brand name suffix
- 6X
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POTASSIUM SULFATE | 6 [hp_X]/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 1K573LC5TV |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76472-4094-1 | KALI SULPHURICUM6X | 80 in 1 CYLINDER | PELLET | 80 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76472-4094 | KALI SULPHURICUM 6X (KALI SULPHURICUM) PELLET [SEVENE USA] | 4 | Current NDC, 1 package rows | 20250213_ff0efbc2-d7ab-9783-e053-6394a90a384f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 76472-4094-1 | 76472409401 | 80 PELLET in 1 CYLINDER (76472-4094-1) | 80 pellet | 2023-06-26 | No | No | Current |