Kali Telluricosum

Product NDC
37662-3341
11-digit product format
376623341
Labeler code
37662
Product ID
37662-3341_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
1 [hp_M]/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 Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
71M41949N8POTASSIUM TELLURITE7790-58-1POTASSIUM TELLURITE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-3341-137662334101200 PELLET in 1 VIAL, GLASS (37662-3341-1) 200 pellet2023-06-08NoNoHistorical
37662-3341-237662334102500 PELLET in 1 VIAL, GLASS (37662-3341-2) 500 pellet2023-06-08NoNoHistorical
37662-3341-3376623341033000 PELLET in 1 BOTTLE, GLASS (37662-3341-3) 3000 pellet2023-06-08NoNoHistorical
37662-3341-43766233410410000 PELLET in 1 BOTTLE, GLASS (37662-3341-4) 10000 pellet2023-06-08NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Kali Telluricosum - Hahnemann Laboratories, INC.Hahnemann Laboratories, INC.2023-06-08HUMAN OTC DRUG LABEL1