Home NDC 63083-5001-2 Adrenal Drops
Product NDC 63083-5001
Requested package NDC 63083-5001-2
11-digit product format 630835001
Labeler code 63083
Product ID 63083-5001_44575f57-e9a9-405e-9de7-2491bf12aa0d
Type HUMAN OTC DRUG
Nonproprietary name Adrenal Drops
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance MILK THISTLE; GINGER; ECHINACEA PURPUREA WHOLE; BERBERIS VULGARIS ROOT BARK; CHELIDONIUM MAJUS WHOLE; BRYONIA ALBA ROOT; SUS SCROFA ADRENAL GLAND; BOS TAURUS SPLEEN; ATROPINE SULFATE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; SILVER NITRATE; LYCOPODIUM CLAVATUM SPORE
Active strength 2; 2; 2; 3; 3; 4; 6; 6; 6; 8; 9; 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; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes Allergens [CS], Anticholinergic [EPC], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
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 Adrenal Drops
Brand name suffix 5001
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MILK THISTLE 2 [hp_X]/59mL GINGER 2 [hp_X]/59mL ECHINACEA PURPUREA WHOLE 2 [hp_X]/59mL BERBERIS VULGARIS ROOT BARK 3 [hp_X]/59mL CHELIDONIUM MAJUS WHOLE 3 [hp_X]/59mL BRYONIA ALBA ROOT 4 [hp_X]/59mL SUS SCROFA ADRENAL GLAND 6 [hp_X]/59mL BOS TAURUS SPLEEN 6 [hp_X]/59mL ATROPINE SULFATE 6 [hp_X]/59mL MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 8 [hp_X]/59mL SILVER NITRATE 9 [hp_X]/59mL LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 12 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 HAD 2026-01-08 HAD 2024-01-30 HAD 2024-01-30 HAD
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-5001-2 Adrenal Drops5001 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 63083-5001 ADRENAL DROPS 5001 (ADRENAL DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220211_9c120843-c43b-4a60-8eaa-d3a951e32ee4.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 63083-5001-2 63083500102 59 mL in 1 BOTTLE, DROPPER (63083-5001-2) 59 ml 1985-08-15 0000-00-00 No No Current