Kali Telluricosum
- Product NDC
- 37662-3335
- 11-digit product format
- 376623335
- Labeler code
- 37662
- Product ID
- 37662-3335_fda9b1e2-9b93-4782-e053-6394a90ac8d3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Kali Telluricosum
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Hahnemann Laboratories, INC.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2023-06-08
- Substance
- POTASSIUM TELLURITE
- Active strength
- 6 [hp_C]/1
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 71M41949N8 | POTASSIUM TELLURITE | 7790-58-1 | POTASSIUM TELLURITE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 37662-3335-1 | 37662333501 | 200 PELLET in 1 VIAL, GLASS (37662-3335-1) | 200 pellet | 2023-06-08 | No | No | Historical |
| 37662-3335-2 | 37662333502 | 1200 PELLET in 1 BOTTLE, GLASS (37662-3335-2) | 1200 pellet | 2023-06-08 | No | No | Historical |
| 37662-3335-3 | 37662333503 | 4000 PELLET in 1 BOTTLE, GLASS (37662-3335-3) | 4000 pellet | 2023-06-08 | No | No | Historical |