Home NDC 63083-9220-1 Crataegus Combination
Product NDC 63083-9220
Requested package NDC 63083-9220-1
11-digit product format 630839220
Labeler code 63083
Product ID 63083-9220_a4cf1cd9-4742-4698-95a6-d7601dda94ea
Type HUMAN OTC DRUG
Nonproprietary name Crataegus Combination
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance HAWTHORN LEAF WITH FLOWER; SPIGELIA ANTHELMIA WHOLE; POTASSIUM CARBONATE; ARNICA MONTANA WHOLE; SELENICEREUS GRANDIFLORUS STEM; GELSEMIUM SEMPERVIRENS ROOT; CASTOR FIBER SCENT GLAND SECRETION; NITROGLYCERIN; RANUNCULUS BULBOSUS WHOLE; SULFUR
Active strength 1; 2; 3; 4; 4; 4; 6; 6; 6; 12 [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 Nitrate Vasodilator [EPC], Nitrates [CS], Vasodilation [PE]
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 Crataegus Combination
Brand name suffix 9220
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HAWTHORN LEAF WITH FLOWER 1 [hp_X]/29.5mL SPIGELIA ANTHELMIA WHOLE 2 [hp_X]/29.5mL POTASSIUM CARBONATE 3 [hp_X]/29.5mL ARNICA MONTANA WHOLE 4 [hp_X]/29.5mL SELENICEREUS GRANDIFLORUS STEM 4 [hp_X]/29.5mL GELSEMIUM SEMPERVIRENS ROOT 4 [hp_X]/29.5mL CASTOR FIBER SCENT GLAND SECRETION 6 [hp_X]/29.5mL NITROGLYCERIN 6 [hp_X]/29.5mL RANUNCULUS BULBOSUS WHOLE 6 [hp_X]/29.5mL SULFUR 12 [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.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# Effective, Related label table Effective Related label 2026-01-09 R220 2026-01-09 R220 2024-01-30 R220 2024-01-30 R220
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-9220-1 Crataegus Combination9220 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 63083-9220 CRATAEGUS COMBINATION 9220 (CRATAEGUS COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220210_ad44d561-9004-43f1-8271-ef52b715fa66.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 63083-9220-1 63083922001 29.5 mL in 1 BOTTLE, DROPPER (63083-9220-1) 29.5 ml 1985-08-15 0000-00-00 No No Current