Home NDC 63083-9256-1 Aralia Combination
Product NDC 63083-9256
Requested package NDC 63083-9256-1
11-digit product format 630839256
Labeler code 63083
Product ID 63083-9256_79c2dbf6-f2b4-4358-879b-16cf5386c412
Type HUMAN OTC DRUG
Nonproprietary name Aralia Combination
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance AMERICAN GINSENG; AVENA SATIVA FLOWERING TOP; YOHIMBINE; GALIUM APARINE WHOLE; SEMPERVIVUM TECTORUM LEAF; AVISCUMINE; CINCHONA OFFICINALIS BARK; COLCHICUM AUTUMNALE BULB; CONIUM MACULATUM FLOWERING TOP; GOLDENSEAL; WOOD CREOSOTE; PULSATILLA MONTANA WHOLE; SULFUR; SCABIES LESION LYSATE (HUMAN)
Active strength 1; 3; 3; 8; 8; 8; 10; 10; 10; 10; 10; 10; 10; 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
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 Aralia Combination
Brand name suffix 9256
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AMERICAN GINSENG 1 [hp_X]/29.5mL AVENA SATIVA FLOWERING TOP 3 [hp_X]/29.5mL YOHIMBINE 3 [hp_X]/29.5mL GALIUM APARINE WHOLE 8 [hp_X]/29.5mL SEMPERVIVUM TECTORUM LEAF 8 [hp_X]/29.5mL AVISCUMINE 8 [hp_X]/29.5mL CINCHONA OFFICINALIS BARK 10 [hp_X]/29.5mL COLCHICUM AUTUMNALE BULB 10 [hp_X]/29.5mL CONIUM MACULATUM FLOWERING TOP 10 [hp_X]/29.5mL GOLDENSEAL 10 [hp_X]/29.5mL WOOD CREOSOTE 10 [hp_X]/29.5mL PULSATILLA MONTANA WHOLE 10 [hp_X]/29.5mL SULFUR 10 [hp_X]/29.5mL SCABIES LESION LYSATE (HUMAN) 30 [hp_X]/29.5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 14 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 2026-01-09 R256 2026-01-09 R256 2024-01-30 R256 2024-01-30 R256
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-9256-1 Aralia Combination9256 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 63083-9256 ARALIA COMBINATION 9256 (ARALIA COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220210_c7248bb6-187d-4076-85dd-94753f7da3b5.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 63083-9256-1 63083925601 29.5 mL in 1 BOTTLE, DROPPER (63083-9256-1) 29.5 ml 1985-08-15 0000-00-00 No No Current