Home NDC 71753-8005-1 Kali Muriaticum
Product NDC 71753-8005
Requested package NDC 71753-8005-1
11-digit product format 717538005
Labeler code 71753
Product ID 71753-8005_fe104583-be74-40ea-a8d9-e1843a552893
Type HUMAN OTC DRUG
Nonproprietary name Kali Muriaticum
Dosage form SPRAY
Route ORAL
Labeler Ratis, LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2020-10-01
Marketing end 2025-10-27
Substance POTASSIUM CHLORIDE
Active strength 6 [hp_X]/mL
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 0000-00-00
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 71753-8005 71753-8005-1 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71753-8005 KALI MURIATICUM SPRAY [RATIS, LLC] 2 Legacy NDC 20220121_ae82bd5a-af81-4376-841d-888faffb120e.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71753-8005-1 71753800501 30 mL in 1 BOTTLE, SPRAY (71753-8005-1) 30 ml 2020-10-01 2025-10-27 No No Current