Kali Sulph
- Product NDC
- 44911-0354
- 11-digit product format
- 449110354
- Labeler code
- 44911
- Product ID
- 44911-0354_b02781c3-88ae-45fe-96e0-5aa3f064ff25
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Kali Sulphuricum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-04-14
- Marketing end
- 2022-09-03
- Substance
- POTASSIUM SULFATE
- Active strength
- 30 [hp_C]/mL
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 44911-0354-1 | 44911035401 | 30 mL in 1 BOTTLE, DROPPER (44911-0354-1) | 30 ml | 2016-04-14 | 0000-00-00 | No | No | Current |