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 ATROPINE SULFATE; BERBERIS VULGARIS ROOT BARK; BOS TAURUS SPLEEN; BRYONIA ALBA ROOT; CHELIDONIUM MAJUS WHOLE; ECHINACEA PURPUREA WHOLE; GINGER; LYCOPODIUM CLAVATUM SPORE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; MILK THISTLE; SILVER NITRATE; SUS SCROFA ADRENAL GLAND
Active strength 6; 3; 6; 4; 3; 2; 2; 12; 8; 2; 9; 6 [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 openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
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 6 [hp_X]/59mL GINGER 3 [hp_X]/59mL ECHINACEA PURPUREA WHOLE 6 [hp_X]/59mL BERBERIS VULGARIS ROOT BARK 4 [hp_X]/59mL CHELIDONIUM MAJUS WHOLE 3 [hp_X]/59mL BRYONIA ALBA ROOT 2 [hp_X]/59mL SUS SCROFA ADRENAL GLAND 2 [hp_X]/59mL BOS TAURUS SPLEEN 12 [hp_X]/59mL ATROPINE SULFATE 8 [hp_X]/59mL MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 2 [hp_X]/59mL SILVER NITRATE 9 [hp_X]/59mL LYCOPODIUM CLAVATUM SPORE 6 [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# 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
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