Home NDC 63083-9257-1 Ledum Combination
Product NDC 63083-9257
Requested package NDC 63083-9257-1
11-digit product format 630839257
Labeler code 63083
Product ID 63083-9257_d444afc7-9686-4d89-888d-a9c48c9192bf
Type HUMAN OTC DRUG
Nonproprietary name Ledum Combination
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance PSEUDOGNAPHALIUM OBTUSIFOLIUM WHOLE; BERBERIS VULGARIS ROOT BARK; BLACK COHOSH; CINCHONA OFFICINALIS BARK; RHODODENDRON TOMENTOSUM LEAFY TWIG; RANUNCULUS BULBOSUS WHOLE; HORSE CHESTNUT; SODIUM BORATE; CITRULLUS COLOCYNTHIS FRUIT PULP; CUPRIC ACETATE; POTASSIUM CARBONATE; PICRIC ACID; PULSATILLA MONTANA WHOLE; CLAVICEPS PURPUREA SCLEROTIUM; SILICON DIOXIDE; AMMONIUM CATION; BOS TAURUS BONE MARROW; BOVINE TYPE II COLLAGEN (TRACHEAL CARTILAGE); BOS TAURUS INTERVERTEBRAL DISC; SUS SCROFA ADRENAL GLAND; SILVER; ANHYDROUS DIBASIC CALCIUM PHOSPHATE; MERCURIC OXIDE; SEPIA OFFICINALIS JUICE; ZINC; GONORRHEAL URETHRAL SECRETION HUMAN; SULFUR
Active strength 3; 4; 4; 4; 4; 4; 6; 6; 6; 6; 6; 6; 6; 6; 6; 8; 8; 8; 8; 10; 10; 10; 10; 10; 10; 12; 30 [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL
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 Ledum Combination
Brand name suffix 9257
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PSEUDOGNAPHALIUM OBTUSIFOLIUM WHOLE 3 [hp_X]/29.5mL BERBERIS VULGARIS ROOT BARK 4 [hp_X]/29.5mL BLACK COHOSH 4 [hp_X]/29.5mL CINCHONA OFFICINALIS BARK 4 [hp_X]/29.5mL RHODODENDRON TOMENTOSUM LEAFY TWIG 4 [hp_X]/29.5mL RANUNCULUS BULBOSUS WHOLE 4 [hp_X]/29.5mL HORSE CHESTNUT 6 [hp_X]/29.5mL SODIUM BORATE 6 [hp_X]/29.5mL CITRULLUS COLOCYNTHIS FRUIT PULP 6 [hp_X]/29.5mL CUPRIC ACETATE 6 [hp_X]/29.5mL POTASSIUM CARBONATE 6 [hp_X]/29.5mL PICRIC ACID 6 [hp_X]/29.5mL PULSATILLA MONTANA WHOLE 6 [hp_X]/29.5mL CLAVICEPS PURPUREA SCLEROTIUM 6 [hp_X]/29.5mL SILICON DIOXIDE 6 [hp_X]/29.5mL AMMONIUM CATION 8 [hp_X]/29.5mL BOS TAURUS BONE MARROW 8 [hp_X]/29.5mL BOVINE TYPE II COLLAGEN (TRACHEAL CARTILAGE) 8 [hp_X]/29.5mL BOS TAURUS INTERVERTEBRAL DISC 8 [hp_X]/29.5mL SUS SCROFA ADRENAL GLAND 10 [hp_X]/29.5mL SILVER 10 [hp_X]/29.5mL ANHYDROUS DIBASIC CALCIUM PHOSPHATE 10 [hp_X]/29.5mL MERCURIC OXIDE 10 [hp_X]/29.5mL SEPIA OFFICINALIS JUICE 10 [hp_X]/29.5mL ZINC 10 [hp_X]/29.5mL GONORRHEAL URETHRAL SECRETION HUMAN 12 [hp_X]/29.5mL SULFUR 30 [hp_X]/29.5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 2 · 27 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 R257 2026-01-09 R257 2024-01-30 R257 2024-01-30 R257
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-9257-1 Ledum Combination9257 29.5 mL in 1 BOTTLE, DROPPER LIQUID 29.5 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63083-9257 LEDUM COMBINATION 9257 (LEDUM COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220210_38b89b32-4915-487d-8b2d-250123487b15.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 63083-9257-1 63083925701 29.5 mL in 1 BOTTLE, DROPPER (63083-9257-1) 29.5 ml 1985-08-15 0000-00-00 No No Current