Home NDC 63083-9226-1 Hamamelis Combination
Product NDC 63083-9226
Requested package NDC 63083-9226-1
11-digit product format 630839226
Labeler code 63083
Product ID 63083-9226_85fe5b8b-daa6-4728-9f53-c756f8c8caea
Type HUMAN OTC DRUG
Nonproprietary name Hamamelis Combination
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance BARIUM CHLORIDE DIHYDRATE; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; MILK THISTLE
Active strength 6; 2; 6 [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…
Additional Listing Data#
Finished product Yes
Brand name base Hamamelis Combination
Brand name suffix 9226
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 6 [hp_X]/29.5mL BARIUM CHLORIDE DIHYDRATE 2 [hp_X]/29.5mL MILK THISTLE 6 [hp_X]/29.5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination T7S323PKJS Internal UNII lookup EL5GJ3U77E Internal UNII lookup U946SH95EE Internal UNII lookup
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 R226 2026-01-09 R226 2024-01-30 R226 2024-01-30 R226
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-9226-1 Hamamelis Combination9226 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 63083-9226 HAMAMELIS COMBINATION 9226 (HAMAMELIS COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220210_48c5ebe9-a0a5-4da5-bcab-3e9f002c6359.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 63083-9226-1 63083922601 29.5 mL in 1 BOTTLE, DROPPER (63083-9226-1) 29.5 ml 1985-08-15 0000-00-00 No No Current