Home NDC 63083-9215-1 Carduus Combination
Product NDC 63083-9215
Requested package NDC 63083-9215-1
11-digit product format 630839215
Labeler code 63083
Product ID 63083-9215_ae0fa92b-a8de-42f3-ade8-e28973a04830
Type HUMAN OTC DRUG
Nonproprietary name Carduus Combination
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance AMARYLLIS BELLADONNA WHOLE; CHOLESTEROL; SULFUR; OYSTER SHELL CALCIUM CARBONATE, CRUDE; MILK THISTLE; CHELIDONIUM MAJUS WHOLE; CINCHONA OFFICINALIS BARK; LYCOPODIUM CLAVATUM SPORE; TARAXACUM OFFICINALE; VERATRUM ALBUM ROOT
Active strength 10; 10; 10; 10; 10; 10; 10; 10; 10; 10 [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 Carduus Combination
Brand name suffix 9215
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AMARYLLIS BELLADONNA WHOLE 10 [hp_X]/29.5mL CHOLESTEROL 10 [hp_X]/29.5mL SULFUR 10 [hp_X]/29.5mL OYSTER SHELL CALCIUM CARBONATE, CRUDE 10 [hp_X]/29.5mL MILK THISTLE 10 [hp_X]/29.5mL CHELIDONIUM MAJUS WHOLE 10 [hp_X]/29.5mL CINCHONA OFFICINALIS BARK 10 [hp_X]/29.5mL LYCOPODIUM CLAVATUM SPORE 10 [hp_X]/29.5mL TARAXACUM OFFICINALE 10 [hp_X]/29.5mL VERATRUM ALBUM ROOT 10 [hp_X]/29.5mL
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.
FDA-Initiated Inactive NDC Indexing# Effective, Related label table Effective Related label 2026-01-09 R215 2026-01-09 R215 2024-01-30 R215 2024-01-30 R215
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-9215-1 Carduus Combination9215 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 63083-9215 CARDUUS COMBINATION 9215 (CARDUUS COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220210_a244de13-836f-49b5-8c7a-d45bde704d78.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 63083-9215-1 63083921501 29.5 mL in 1 BOTTLE, DROPPER (63083-9215-1) 29.5 ml 1985-08-15 0000-00-00 No No Current