Home NDC 0220-2943 Kreosotum
Product NDC 0220-2943
11-digit product format 002202943
Labeler code 0220
Product ID 0220-2943_f52c22b6-878a-deb8-e053-2a95a90a1aaa
Type HUMAN OTC DRUG
Nonproprietary name WOOD CREOSOTE
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance WOOD CREOSOTE
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 Kreosotum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength WOOD CREOSOTE 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 3JYG22FD73 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 0220-2943-41 Kreosotum 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 0220-2943 KREOSOTUM (WOOD CREOSOTE ) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20230222_8619af2a-49b8-0953-e053-2991aa0a01d1.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 0220-2943-41 00220294341 30 [hp_C] in 1 TUBE (0220-2943-41) 1983-03-03 0000-00-00 No No Current