Home NDC 63083-2029-2 Hyperthyroid Drops
Product NDC 63083-2029
Requested package NDC 63083-2029-2
11-digit product format 630832029
Labeler code 63083
Product ID 63083-2029_289f2400-c0ff-4e74-9fc4-e7979e0b8970
Type HUMAN OTC DRUG
Nonproprietary name Hyperthyroid Drops
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance POTASSIUM IODIDE; LYCOPUS VIRGINICUS WHOLE; APIS MELLIFERA; ACTIVATED CHARCOAL; SPONGIA OFFICINALIS SKELETON, ROASTED; CONIUM MACULATUM FLOWERING TOP; PHOSPHORUS; BOS TAURUS PITUITARY GLAND, POSTERIOR; LACHESIS MUTA VENOM
Active strength 2; 2; 3; 3; 4; 6; 6; 6; 8 [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…
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 Hyperthyroid Drops
Brand name suffix 2029
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM IODIDE 2 [hp_X]/59mL LYCOPUS VIRGINICUS WHOLE 2 [hp_X]/59mL APIS MELLIFERA 3 [hp_X]/59mL ACTIVATED CHARCOAL 3 [hp_X]/59mL SPONGIA OFFICINALIS SKELETON, ROASTED 4 [hp_X]/59mL CONIUM MACULATUM FLOWERING TOP 6 [hp_X]/59mL PHOSPHORUS 6 [hp_X]/59mL BOS TAURUS PITUITARY GLAND, POSTERIOR 6 [hp_X]/59mL LACHESIS MUTA VENOM 8 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 9 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 2026-01-08 C29 2026-01-08 C29 2024-01-30 C29 2024-01-30 C29
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-2029-2 Hyperthyroid Drops2029 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 63083-2029 HYPERTHYROID DROPS 2029 (HYPERTHYROID DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220215_be6f64dd-946b-4933-abb7-7b4c095c2490.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 63083-2029-2 63083202902 59 mL in 1 BOTTLE, DROPPER (63083-2029-2) 59 ml 1985-08-15 0000-00-00 No No Current