Kali Chloricum

Product NDC
37662-0879
11-digit product format
376620879
Labeler code
37662
Product ID
37662-0879_e3baf111-d3e8-7f7f-e053-2995a90a84e6
Type
HUMAN OTC DRUG
Nonproprietary name
Kali Chloricum
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-07-13
Substance
POTASSIUM CHLORATE
Active strength
200 [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 Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
H35KS68EE7POTASSIUM CHLORATE3811-04-9POTASSIUM CHLORATE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-0879-137662087901200 PELLET in 1 VIAL, GLASS (37662-0879-1) 200 pellet2022-07-13NoNoHistorical
37662-0879-237662087902500 PELLET in 1 VIAL, GLASS (37662-0879-2) 500 pellet2022-07-13NoNoHistorical
37662-0879-3376620879033000 PELLET in 1 BOTTLE, GLASS (37662-0879-3) 3000 pellet2022-07-13NoNoHistorical
37662-0879-43766208790410000 PELLET in 1 BOTTLE, GLASS (37662-0879-4) 10000 pellet2022-07-13NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Kali Chloricum - Hahnemann Laboratories, INC.Hahnemann Laboratories, INC.2022-07-13HUMAN OTC DRUG LABEL1