Home NDC 71753-8006 Kali Phosphoricum
Product NDC 71753-8006
11-digit product format 717538006
Labeler code 71753
Product ID 71753-8006_7ceb50eb-2adc-465b-a931-bef6ca6af7f7
Type HUMAN OTC DRUG
Nonproprietary name Kali Phosphoricum
Dosage form SPRAY
Route ORAL
Labeler Ratis, LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2020-09-30
Substance DIBASIC POTASSIUM PHOSPHATE
Active strength 6 [hp_X]/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Kali Phosphoricum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIBASIC POTASSIUM PHOSPHATE 6 [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 71753-8006-1 Kali Phosphoricum 30 mL in 1 BOTTLE, SPRAY SPRAY 30 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71753-8006 KALI PHOSPHORICUM SPRAY [RATIS, LLC] 3 Current NDC, Legacy NDC, 1 package rows 20230526_43284190-e5b0-4561-9e7a-f84d374d5913.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 Marketing end Sample Exclude flag Status 71753-8006-1 71753800601 30 mL in 1 BOTTLE, SPRAY (71753-8006-1) 30 ml 2020-09-30 0000-00-00 No No Current