Kali Sulphuricum
- Product NDC
- 71753-8007
- 11-digit product format
- 717538007
- Labeler code
- 71753
- Product ID
- 71753-8007_755dd085-e530-4320-a574-299151cc654a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Kali Sulphuricum
- Dosage form
- SPRAY
- Route
- ORAL
- Labeler
- Ratis, LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2020-09-30
- Substance
- POTASSIUM SULFATE
- Active strength
- 6 [hp_X]/mL
- Pharmacologic classes
- Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [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
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POTASSIUM SULFATE | 6 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 1K573LC5TV |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71753-8007-1 | Kali Sulphuricum | 30 mL in 1 BOTTLE, SPRAY | SPRAY | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71753-8007 | KALI SULPHURICUM SPRAY [RATIS, LLC] | 3 | Current NDC, Legacy NDC, 1 package rows | 20230714_f0061e89-ff0e-452e-9a9c-ee24020b3e88.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71753-8007-1 | 71753800701 | 30 mL in 1 BOTTLE, SPRAY (71753-8007-1) | 30 ml | 2020-09-30 | 2025-10-28 | No | No | Current |