Home NDC 63083-2080-2 Gout Drops
Product NDC 63083-2080
Requested package NDC 63083-2080-2
11-digit product format 630832080
Labeler code 63083
Product ID 63083-2080_de14e93f-43cf-4282-9aa8-58808df90c38
Type HUMAN OTC DRUG
Nonproprietary name Gout Drops
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance BRYONIA ALBA ROOT; SOLANUM DULCAMARA WHOLE; RHODODENDRON TOMENTOSUM LEAFY TWIG; ARNICA MONTANA WHOLE; BENZOIC ACID; COLCHICUM AUTUMNALE BULB; LITHIUM CARBONATE; URTICA URENS WHOLE; FORMICA RUFA; LYCOPODIUM CLAVATUM SPORE
Active strength 4; 4; 4; 6; 6; 6; 6; 6; 12; 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 Ammonium Ion Binding Activity [MoA], Mood Stabilizer [EPC], Nitrogen Binding Agent [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 Gout Drops
Brand name suffix 2080
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BRYONIA ALBA ROOT 4 [hp_X]/59mL SOLANUM DULCAMARA WHOLE 4 [hp_X]/59mL RHODODENDRON TOMENTOSUM LEAFY TWIG 4 [hp_X]/59mL ARNICA MONTANA WHOLE 6 [hp_X]/59mL BENZOIC ACID 6 [hp_X]/59mL COLCHICUM AUTUMNALE BULB 6 [hp_X]/59mL LITHIUM CARBONATE 6 [hp_X]/59mL URTICA URENS WHOLE 6 [hp_X]/59mL FORMICA RUFA 12 [hp_X]/59mL LYCOPODIUM CLAVATUM SPORE 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.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# Effective, Related label table Effective Related label 2026-01-09 C80 2026-01-09 C80 2024-01-30 C80 2024-01-30 C80
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-2080-2 Gout Drops2080 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 63083-2080 GOUT DROPS 2080 (GOUT DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220215_30696295-01f6-4a50-a932-76fdc7c0501a.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 63083-2080-2 63083208002 59 mL in 1 BOTTLE, DROPPER (63083-2080-2) 59 ml 1985-08-15 0000-00-00 No No Current