Home NDC 63083-9202-1 Aesculus Combination
Product NDC 63083-9202
Requested package NDC 63083-9202-1
11-digit product format 630839202
Labeler code 63083
Product ID 63083-9202_fd8dfec8-ce8a-40dc-a315-a6f117bc6d53
Type HUMAN OTC DRUG
Nonproprietary name Aesculus Combination
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance HORSE CHESTNUT; ECHINACEA ANGUSTIFOLIA WHOLE; ARNICA MONTANA WHOLE; CLAVICEPS PURPUREA SCLEROTIUM; AVISCUMINE; APIS MELLIFERA; BAPTISIA TINCTORIA WHOLE; BENZOIC ACID; COLCHICUM AUTUMNALE BULB; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; RUTA GRAVEOLENS FLOWERING TOP; BARIUM IODIDE; EUPATORIUM PERFOLIATUM FLOWERING TOP; TOXICODENDRON PUBESCENS LEAF; SOLANUM NIGRUM TOP; SODIUM PYRUVATE; BEEF HEART; TOBACCO LEAF; COPPER; SULFUR
Active strength 1; 2; 3; 3; 3; 4; 4; 4; 4; 4; 4; 6; 6; 6; 6; 8; 10; 10; 13; 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
Pharmacologic classes Allergens [CS], Allergens [CS], Ammonium Ion Binding Activity [MoA], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Nitrogen Binding Agent [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Standardized Insect Venom Allergenic Extract [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 Aesculus Combination
Brand name suffix 9202
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HORSE CHESTNUT 1 [hp_X]/29.5mL ECHINACEA ANGUSTIFOLIA WHOLE 2 [hp_X]/29.5mL ARNICA MONTANA WHOLE 3 [hp_X]/29.5mL CLAVICEPS PURPUREA SCLEROTIUM 3 [hp_X]/29.5mL AVISCUMINE 3 [hp_X]/29.5mL APIS MELLIFERA 4 [hp_X]/29.5mL BAPTISIA TINCTORIA WHOLE 4 [hp_X]/29.5mL BENZOIC ACID 4 [hp_X]/29.5mL COLCHICUM AUTUMNALE BULB 4 [hp_X]/29.5mL HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 4 [hp_X]/29.5mL RUTA GRAVEOLENS FLOWERING TOP 4 [hp_X]/29.5mL BARIUM IODIDE 6 [hp_X]/29.5mL EUPATORIUM PERFOLIATUM FLOWERING TOP 6 [hp_X]/29.5mL TOXICODENDRON PUBESCENS LEAF 6 [hp_X]/29.5mL SOLANUM NIGRUM TOP 6 [hp_X]/29.5mL SODIUM PYRUVATE 8 [hp_X]/29.5mL BEEF HEART 10 [hp_X]/29.5mL TOBACCO LEAF 10 [hp_X]/29.5mL COPPER 13 [hp_X]/29.5mL SULFUR 30 [hp_X]/29.5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 20 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 R202 2026-01-09 R202 2024-01-30 R202 2024-01-30 R202
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-9202-1 Aesculus Combination9202 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 63083-9202 AESCULUS COMBINATION 9202 (AESCULUS COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220210_5318d83a-2d8f-4ecc-80ac-d191be5f198f.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 63083-9202-1 63083920201 29.5 mL in 1 BOTTLE, DROPPER (63083-9202-1) 29.5 ml 1985-08-15 0000-00-00 No No Current