Home NDC 71919-766-01 Eupatorium Perf Kit Refill
Product NDC 71919-766
Requested package NDC 71919-766-01
11-digit product format 719190766
Labeler code 71919
Product ID 71919-766_2cc7eaac-d564-efae-e063-6394a90aeee8
Type HUMAN OTC DRUG
Nonproprietary name Eupatorium Perfoliatum Flowering Top
Dosage form PELLET
Route ORAL
Labeler Washington Homeopathic Products
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2022-05-25
Substance EUPATORIUM PERFOLIATUM FLOWERING TOP
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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 71919-766 71919-766-01 U Excluded because listing certification expired excluded / ndc_excluded.zip ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 71919-766 71919-766-01 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
Additional Listing Data#
Finished product Yes
Brand name base Eupatorium Perf Kit Refill
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength EUPATORIUM PERFOLIATUM FLOWERING TOP 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 1W0775VX6E 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 71919-766-01 Eupatorium Perf Kit Refill 350 in 1 VIAL, GLASS PELLET 350 4 71919-766-01 Complete 30C/200C Homeopathic Kit 350 in 1 VIAL, GLASS PELLET 350 200 [hp_C] 2 71919-766-01 200C Homeopathic Remedy Kit 350 in 1 VIAL, GLASS PELLET 350 200 [hp_C] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71919-766 EUPATORIUM PERF KIT REFILL (EUPATORIUM PERFOLIATUM FLOWERING TOP) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS] 4 Current NDC, Legacy NDC, 1 package rows 20250130_dfdacffb-81d9-8343-e053-2995a90a7627.zip 71919-766 200C HOMEOPATHIC REMEDY KIT (50 REMEDY KIT) KIT [WASHINGTON HOMEOPATHIC PRODUCTS] 1 Current NDC, Legacy NDC 20240307_1287230a-0842-95df-e063-6294a90a0d60.zip 71919-766 COMPLETE 30C/200C HOMEOPATHIC KIT (100 REMEDY KIT) KIT [WASHINGTON HOMEOPATHIC PRODUCTS] 1 Current NDC, Legacy NDC 20240516_16ecc94f-1001-983c-e063-6294a90a7b6c.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 · 2 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 71919-766-01 71919076601 350 PELLET in 1 VIAL, GLASS (71919-766-01) 350 pellet 2022-05-25 0000-00-00 No No Current