Home NDC 63083-5027-2 Thymus Drops
Product NDC 63083-5027
Requested package NDC 63083-5027-2
11-digit product format 630835027
Labeler code 63083
Product ID 63083-5027_1d47c388-6c8f-490d-a906-aac337ef3903
Type HUMAN OTC DRUG
Nonproprietary name Thymus Drops
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance AMARYLLIS BELLADONNA WHOLE; ARSENIC TRIOXIDE; BOS TAURUS BONE MARROW; BOS TAURUS SPLEEN; CALCIUM FLUORIDE; CALCIUM SULFATE ANHYDROUS; CALCIUM SULFIDE; ECHINACEA PURPUREA WHOLE; HYSSOPUS OFFICINALIS WHOLE; LACHESIS MUTA VENOM; SILICON DIOXIDE; SULFUR IODIDE; VIROLA SEBIFERA RESIN
Active strength 6; 6; 6; 6; 6; 4; 8; 1; 6; 12; 6; 6; 3 [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; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
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 Thymus Drops
Brand name suffix 5027
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ECHINACEA PURPUREA WHOLE 6 [hp_X]/59mL VIROLA SEBIFERA RESIN 6 [hp_X]/59mL CALCIUM SULFATE ANHYDROUS 6 [hp_X]/59mL ARSENIC TRIOXIDE 6 [hp_X]/59mL AMARYLLIS BELLADONNA WHOLE 6 [hp_X]/59mL BOS TAURUS BONE MARROW 4 [hp_X]/59mL CALCIUM FLUORIDE 8 [hp_X]/59mL SILICON DIOXIDE 1 [hp_X]/59mL BOS TAURUS SPLEEN 6 [hp_X]/59mL SULFUR IODIDE 12 [hp_X]/59mL HYSSOPUS OFFICINALIS WHOLE 6 [hp_X]/59mL CALCIUM SULFIDE 6 [hp_X]/59mL LACHESIS MUTA VENOM 3 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 13 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# Effective, Related label table Effective Related label 2026-01-08 HTMD 2026-01-08 HTMD 2024-01-30 HTMD 2024-01-30 HTMD
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-5027-2 Thymus Drops5027 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 63083-5027 THYMUS DROPS 5027 (THYMUS DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220211_8d7c42f7-02ae-4992-986f-4743151ad3bb.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 63083-5027-2 63083502702 59 mL in 1 BOTTLE, DROPPER (63083-5027-2) 59 ml 1985-08-15 0000-00-00 No No Current