Home NDC 55714-9014-1 Thuja occidentalis
Product NDC 55714-9014
Requested package NDC 55714-9014-1
11-digit product format 557149014
Labeler code 55714
Product ID 55714-9014_2dd2175c-db42-4df9-e063-6394a90a5e84
Type HUMAN OTC DRUG
Nonproprietary name Thuja occidentalis
Dosage form PELLET
Route ORAL
Labeler Newton Laboratories, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2020-01-01
Substance THUJA OCCIDENTALIS LEAFY TWIG
Active strength 30 [hp_C]/g
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 · 3 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 2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 55714-9014 55714-9014-1 U Excluded because listing certification expired excluded / ndc_excluded.zip 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 55714-9014 55714-9014-1 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 55714-9014 55714-9014-1 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
Additional Listing Data#
Finished product Yes
Brand name base Thuja occidentalis
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength THUJA OCCIDENTALIS LEAFY TWIG 30 [hp_C]/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1NT28V9397 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 55714-9014-1 Thuja occidentalis 28 g in 1 BOTTLE, GLASS PELLET 28 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55714-9014 THUJA OCCIDENTALIS PELLET [NEWTON LABORATORIES, INC.] 2 Current NDC, Legacy NDC, 1 package rows 20250212_9e3ed894-5bfc-b597-e053-2a95a90a8a69.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 55714-9014-1 55714901401 28 g in 1 BOTTLE, GLASS (55714-9014-1) 28 g 2020-01-01 0000-00-00 No No Current