Home NDC 0220-1315 CHININUM ARSENICOSUM
Product NDC 0220-1315
11-digit product format 002201315
Labeler code 0220
Product ID 0220-1315_3b3d0411-e8a1-5525-e063-6394a90ae2c4
Type HUMAN OTC DRUG
Nonproprietary name QUININE ARSENITE
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-01-01
Substance QUININE ARSENITE
Active strength 200 [kp_C]/200[kp_C]
Pharmacologic classes Antimalarial [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base CHININUM ARSENICOSUM
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength QUININE ARSENITE 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 42QO5P0NLM Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0220-1315-41 CHININUM ARSENICOSUM 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 0220-1315-41 00220131541 200 [kp_C] in 1 TUBE (0220-1315-41) 2025-01-01 No No Current