Kali chloricum

Product NDC
0220-2871
11-digit product format
002202871
Labeler code
0220
Product ID
0220-2871_0a0e1efd-9eb7-83d7-e063-6294a90a9643
Type
HUMAN OTC DRUG
Nonproprietary name
POTASSIUM CHLORATE
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
POTASSIUM CHLORATE
Active strength
30 [hp_C]/30[hp_C]
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 formatDescriptionMarketing startSampleExclude flagStatus
0220-2871-410022028714130 [hp_C] in 1 TUBE (0220-2871-41) 1983-03-03NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Kali chloricum 30CBoiron | Boiron, Inc.2023-11-13HUMAN OTC DRUG LABEL3