Home NDC 0220-1465 Coccus cacti
Product NDC 0220-1465
11-digit product format 002201465
Labeler code 0220
Product ID 0220-1465_09bf56c4-6115-7aa8-e063-6394a90ad44b
Type HUMAN OTC DRUG
Nonproprietary name PROTORTONIA CACTI
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance PROTORTONIA CACTI
Active strength 200 [kp_C]/200[kp_C]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Coccus cacti
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PROTORTONIA CACTI 200 [kp_C]/200[kp_C]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination LZB7TFX1LT Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0220-1465-41 Coccus cacti 200 [kp_C] in 1 TUBE PELLET 200 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-1465 COCCUS CACTI (PROTORTONIA CACTI ) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20231110_853c7464-f6cf-2bba-e053-2991aa0a7030.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 Marketing start Marketing end Sample Exclude flag Status 0220-1465-41 00220146541 200 [kp_C] in 1 TUBE (0220-1465-41) 1983-03-03 0000-00-00 No No Current