Home NDC 63083-2154-2 TMJ Drops
Product NDC 63083-2154
Requested package NDC 63083-2154-2
11-digit product format 630832154
Labeler code 63083
Product ID 63083-2154_65fd39b6-f440-4491-acee-338a5993bbfb
Type HUMAN OTC DRUG
Nonproprietary name TMJ Drops
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance AMARYLLIS BELLADONNA WHOLE; APIS MELLIFERA; ARNICA MONTANA WHOLE; BOS TAURUS LIGAMENT; BOVINE TYPE II COLLAGEN (TRACHEAL CARTILAGE); CALCIUM SULFIDE; CICUTA VIROSA WHOLE; POTASSIUM CARBONATE; SPIGELIA ANTHELMIA WHOLE; VERBASCUM THAPSUS WHOLE
Active strength 12; 1; 30; 12; 12; 30; 12; 12; 60; 12 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
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 2027-12-31
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 · 15 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 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…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…
Additional Listing Data#
Finished product Yes
Brand name base TMJ Drops
Brand name suffix 2154
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength APIS MELLIFERA 12 [hp_X]/59mL AMARYLLIS BELLADONNA WHOLE 1 [hp_X]/59mL BOVINE TYPE II COLLAGEN (TRACHEAL CARTILAGE) 30 [hp_X]/59mL CICUTA VIROSA WHOLE 12 [hp_X]/59mL POTASSIUM CARBONATE 12 [hp_X]/59mL BOS TAURUS LIGAMENT 30 [hp_X]/59mL VERBASCUM THAPSUS WHOLE 12 [hp_X]/59mL CALCIUM SULFIDE 12 [hp_X]/59mL ARNICA MONTANA WHOLE 60 [hp_X]/59mL SPIGELIA ANTHELMIA WHOLE 12 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 10 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# Effective, Related label table Effective Related label 2026-01-09 C154 2026-01-09 C154 2024-01-30 C154 2024-01-30 C154
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-2154-2 TMJ Drops2154 59 mL in 1 BOTTLE, DROPPER LIQUID 59 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63083-2154 TMJ DROPS 2154 (TMJ DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220216_a937e0e7-899d-48db-af58-9e0c11d5a24c.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 63083-2154-2 63083215402 59 mL in 1 BOTTLE, DROPPER (63083-2154-2) 59 ml 1985-08-15 0000-00-00 No No Current