Home NDC 71919-765 Baptisia Tinctoria Kit Refill
Product NDC 71919-765
11-digit product format 719190765
Labeler code 71919
Product ID 71919-765_2cc7eaaf-e2c6-f06a-e063-6394a90a1961
Type HUMAN OTC DRUG
Nonproprietary name BAPTISIA TINCTORIA ROOT
Dosage form PELLET
Route ORAL
Labeler Washington Homeopathic Products
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2022-05-10
Substance BAPTISIA TINCTORIA ROOT
Active strength 200 [hp_C]/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 71919-765-01 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 71919-765-01 0efc9e666f02…f202fb6c5f17…
Additional Listing Data#
Finished product Yes
Brand name base Baptisia Tinctoria Kit Refill
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BAPTISIA TINCTORIA ROOT 200 [hp_C]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5EF0HWI5WU 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 71919-765-01 Baptisia Tinctoria Kit Refill 350 in 1 VIAL, GLASS PELLET 350 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71919-765 BAPTISIA TINCTORIA KIT REFILL (BAPTISIA TINCTORIA ROOT) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS] 4 Current NDC, Legacy NDC, 1 package rows 20250130_dead18ed-a4ba-8129-e053-2a95a90a3f2e.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 Units Marketing start Marketing end Sample Exclude flag Status 71919-765-01 71919076501 350 PELLET in 1 VIAL, GLASS (71919-765-01) 350 pellet 2022-05-10 0000-00-00 No No Current