Home NDC 50845-0273-1 Joint plus Tendon
Product NDC 50845-0273
Requested package NDC 50845-0273-1
11-digit product format 508450273
Labeler code 50845
Product ID 50845-0273_4b37fd54-ae68-4a07-816b-6fe304afe2e6
Type HUMAN OTC DRUG
Nonproprietary name Aconitum Napellus, Apis Mellifica, Arnica Montana, Cartilago Suis, Hydrastis Canadensis, Hypericum Perforatum, Rhus Tox, Thuja Occidentalis
Dosage form SPRAY
Route ORAL
Labeler Liddell Laboratories, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2022-06-20
Substance ACONITUM NAPELLUS WHOLE; APIS MELLIFERA; ARNICA MONTANA WHOLE; SUS SCROFA CARTILAGE; GOLDENSEAL; HYPERICUM PERFORATUM WHOLE; TOXICODENDRON PUBESCENS LEAF; THUJA OCCIDENTALIS LEAFY TWIG
Active strength 200; 200; 200; 6; 6; 200; 200; 200 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
Pharmacologic classes Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]
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 · 5 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Joint plus Tendon
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACONITUM NAPELLUS WHOLE 200 [hp_C]/mL APIS MELLIFERA 200 [hp_C]/mL ARNICA MONTANA WHOLE 200 [hp_C]/mL SUS SCROFA CARTILAGE 6 [hp_X]/mL GOLDENSEAL 6 [hp_X]/mL HYPERICUM PERFORATUM WHOLE 200 [hp_C]/mL TOXICODENDRON PUBESCENS LEAF 200 [hp_C]/mL THUJA OCCIDENTALIS LEAFY TWIG 200 [hp_C]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 8 matching rows.
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 50845-0273-1 Joint plus Tendon 30 mL in 1 BOTTLE, SPRAY SPRAY 30 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50845-0273 JOINT PLUS TENDON (ACONITUM NAPELLUS, APIS MELLIFICA, ARNICA MONTANA, CARTILAGO SUIS, HYDRASTIS CANADENSIS, HYPERICUM PERFORATUM, RHUS TOX, THUJA OCCIDENTALIS) SPRAY [LIDDELL LABORATORIES, INC.] 3 Current NDC, Legacy NDC, 1 package rows 20241105_64465f12-f50e-46ef-bb82-9b10b18cfa24.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.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Joint plus Tendon ACONITUM NAPELLUS, APIS MELLIFICA, ARNICA MONTANA, CARTILAGO SUIS, HYDRASTIS CANADENSIS, HYPERICUM PERFORATUM, RHUS TOX, THUJA OCCIDENTALIS Liddell Laboratories, Inc. 64465f12-f50e-46ef-bb82-9b10b18cfa24 2024-11-04 Warnings Exact identifier ndc (package): 50845-0273-1 ndc (product): 50845-0273 ndc11 (package): 50845027301
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 50845-0273-1 50845027301 30 mL in 1 BOTTLE, SPRAY (50845-0273-1) 30 ml 2022-06-20 0000-00-00 No No Current