Home NDC 0220-2833 Kali bichromicum
Product NDC 0220-2833
11-digit product format 002202833
Labeler code 0220
Product ID 0220-2833_f2f62640-92f6-a9c4-e053-2995a90ac842
Type HUMAN OTC DRUG
Nonproprietary name POTASSIUM DICHROMATE
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance POTASSIUM DICHROMATE
Active strength 30 [hp_C]/30[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 Kali bichromicum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM DICHROMATE 30 [hp_C]/30[hp_C]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination T4423S18FM 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 0220-2833-41 Kali bichromicum 30 [hp_C] in 1 TUBE PELLET 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-2833 KALI BICHROMICUM (POTASSIUM DICHROMATE ) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20230124_8605ed85-eed7-a67a-e053-2a91aa0ace8a.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 0220-2833-41 00220283341 30 [hp_C] in 1 TUBE (0220-2833-41) 1983-03-03 0000-00-00 No No Current