Home NDC 63083-9224-1 Geranium Combination
Product NDC 63083-9224
Requested package NDC 63083-9224-1
11-digit product format 630839224
Labeler code 63083
Product ID 63083-9224_4f06c27d-7767-4a09-9831-81efa6700de4
Type HUMAN OTC DRUG
Nonproprietary name Geranium Combination
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance GERANIUM ROBERTIANUM WHOLE; ALOE; COLCHICUM AUTUMNALE BULB; VERATRUM ALBUM ROOT; SILVER NITRATE; ARSENIC TRIOXIDE; CITRULLUS COLOCYNTHIS FRUIT PULP; PODOPHYLLUM; FERROSOFERRIC PHOSPHATE; ANTIMONY TRISULFIDE; MERCURIC CHLORIDE
Active strength 2; 4; 4; 4; 6; 6; 6; 6; 10; 12; 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; [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 Geranium Combination
Brand name suffix 9224
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GERANIUM ROBERTIANUM WHOLE 2 [hp_X]/29.5mL ALOE 4 [hp_X]/29.5mL COLCHICUM AUTUMNALE BULB 4 [hp_X]/29.5mL VERATRUM ALBUM ROOT 4 [hp_X]/29.5mL SILVER NITRATE 6 [hp_X]/29.5mL ARSENIC TRIOXIDE 6 [hp_X]/29.5mL CITRULLUS COLOCYNTHIS FRUIT PULP 6 [hp_X]/29.5mL PODOPHYLLUM 6 [hp_X]/29.5mL FERROSOFERRIC PHOSPHATE 10 [hp_X]/29.5mL ANTIMONY TRISULFIDE 12 [hp_X]/29.5mL MERCURIC CHLORIDE 12 [hp_X]/29.5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 11 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 2026-01-08 R224 2026-01-08 R224 2024-01-30 R224 2024-01-30 R224
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-9224-1 Geranium Combination9224 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 63083-9224 GERANIUM COMBINATION 9224 (GERANIUM COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220210_83c08370-acd7-4540-89fb-473f0761e8cb.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 63083-9224-1 63083922401 29.5 mL in 1 BOTTLE, DROPPER (63083-9224-1) 29.5 ml 1985-08-15 0000-00-00 No No Current