Home NDC 15631-2804-1 KALI PHOS
Product NDC 15631-2804
Requested package NDC 15631-2804-1
11-digit product format 156312804
Labeler code 15631
Product ID 15631-2804_1a3533ed-56a6-c549-e063-6294a90a364d
Type HUMAN OTC DRUG
Nonproprietary name KALI PHOS
Dosage form LIQUID
Route ORAL
Labeler Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2024-05-23
Substance POTASSIUM PHOSPHATE, DIBASIC
Active strength 1 [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 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base KALI PHOS
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM PHOSPHATE, DIBASIC 1 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination CI71S98N1Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 15631-2804-0 KALI PHOS 10 mL in 1 BOTTLE LIQUID 10 1 15631-2804-1 KALI PHOS 30 mL in 1 BOTTLE LIQUID 30 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 15631-2804 KALI PHOS LIQUID [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC] 1 Current NDC, 2 package rows 20240612_1a352e80-4479-13b0-e063-6394a90a7be5.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 15631-2804-1 15631280401 30 mL in 1 BOTTLE (15631-2804-1) 30 ml 2024-05-23 No No Current