Home NDC 0220-7604 Psorinum
Product NDC 0220-7604
11-digit product format 002207604
Labeler code 0220
Product ID 0220-7604_0a35ec95-6aaa-333e-e063-6394a90a4b1b
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name SCABIES LESION LYSATE (HUMAN)
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance SCABIES LESION LYSATE (HUMAN)
Active strength 7 [hp_X]/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Psorinum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SCABIES LESION LYSATE (HUMAN) 7 [hp_X]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5UAU16Z1U4 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 0220-7604-41 Psorinum 80 in 1 TUBE PELLET 80 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-7604 PSORINUM (SCABIES LESION LYSATE (HUMAN)) PELLET [BOIRON] 4 Current NDC, Legacy NDC, 1 package rows 20231116_dd752fa0-bf6b-11e7-8233-424c58303031.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 0220-7604-41 00220760441 80 PELLET in 1 TUBE (0220-7604-41) 80 pellet 1983-03-03 0000-00-00 No No Current