Home NDC 0220-1339 Cholesterinum
Product NDC 0220-1339
11-digit product format 002201339
Labeler code 0220
Product ID 0220-1339_09bf0d69-c1b0-62bb-e063-6394a90abb26
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name CHOLESTEROL
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance CHOLESTEROL
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 Cholesterinum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CHOLESTEROL 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 97C5T2UQ7J 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 0220-1339-41 Cholesterinum 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 0220-1339 CHOLESTERINUM (CHOLESTEROL) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20231110_8529a8cf-5a5f-1eb0-e053-2991aa0aded0.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 0220-1339-41 00220133941 200 [kp_C] in 1 TUBE (0220-1339-41) 1983-03-03 0000-00-00 No No Current