Home NDC 0220-1605 Cuprum arsenicosum
Product NDC 0220-1605
11-digit product format 002201605
Labeler code 0220
Product ID 0220-1605_0a0c4723-3001-0c05-e063-6294a90ac904
Type HUMAN OTC DRUG
Nonproprietary name CUPRIC ARSENITE
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance CUPRIC ARSENITE
Active strength 9 [hp_C]/9[hp_C]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Cuprum arsenicosum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CUPRIC ARSENITE 9 [hp_C]/9[hp_C]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SK8L60BCSQ Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0220-1605-41 Cuprum arsenicosum 9 [hp_C] in 1 TUBE PELLET 9 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-1605 CUPRUM ARSENICOSUM (CUPRIC ARSENITE) PELLET [BOIRON] 3 Current NDC, Legacy NDC, 1 package rows 20231114_7a2e37eb-fbd6-17c4-e053-2a91aa0ad1e4.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 0220-1605-41 00220160541 9 [hp_C] in 1 TUBE (0220-1605-41) 1983-03-03 0000-00-00 No No Current