Home NDC 0220-3651 NICCOLUM METALLICUM
Product NDC 0220-3651
11-digit product format 002203651
Labeler code 0220
Product ID 0220-3651_3b8c8a00-78a0-1909-e063-6394a90addd4
Type HUMAN OTC DRUG
Nonproprietary name NICKEL
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-01-01
Substance NICKEL
Active strength 200 [kp_C]/200[kp_C]
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base NICCOLUM METALLICUM
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength NICKEL 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 7OV03QG267 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0220-3651-41 NICCOLUM METALLICUM 200 [kp_C] in 1 TUBE PELLET 200 1
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 Sample Exclude flag Status 0220-3651-41 00220365141 200 [kp_C] in 1 TUBE (0220-3651-41) 2025-01-01 No No Current