Home NDC 63083-9233-1 Mercurius Combination
Product NDC 63083-9233
Requested package NDC 63083-9233-1
11-digit product format 630839233
Labeler code 63083
Product ID 63083-9233_6807acea-520d-4492-b4cd-03e2d6ef8863
Type HUMAN OTC DRUG
Nonproprietary name Mercurius Combination
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance AILANTHUS ALTISSIMA FLOWERING TWIG; AMARYLLIS BELLADONNA WHOLE; ARSENIC TRIOXIDE; CALCIUM SULFIDE; DAPHNE MEZEREUM BARK; ECHINACEA ANGUSTIFOLIA WHOLE; HUMAN HERPESVIRUS 1; LACHESIS MUTA VENOM; MERCURIUS SOLUBILIS; PHYTOLACCA AMERICANA ROOT; RECOMBINANT VARICELLA ZOSTER VIRUS GLYCOPROTEIN E ANTIGEN
Active strength 3; 4; 12; 8; 9; 3; 12; 12; 12; 4; 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…
Additional Listing Data#
Finished product Yes
Brand name base Mercurius Combination
Brand name suffix 9233
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AILANTHUS ALTISSIMA FLOWERING TWIG 3 [hp_X]/29.5mL ECHINACEA ANGUSTIFOLIA WHOLE 4 [hp_X]/29.5mL AMARYLLIS BELLADONNA WHOLE 12 [hp_X]/29.5mL PHYTOLACCA AMERICANA ROOT 8 [hp_X]/29.5mL CALCIUM SULFIDE 9 [hp_X]/29.5mL DAPHNE MEZEREUM BARK 3 [hp_X]/29.5mL ARSENIC TRIOXIDE 12 [hp_X]/29.5mL HUMAN HERPESVIRUS 1 12 [hp_X]/29.5mL RECOMBINANT VARICELLA ZOSTER VIRUS GLYCOPROTEIN E ANTIGEN 12 [hp_X]/29.5mL LACHESIS MUTA VENOM 4 [hp_X]/29.5mL MERCURIUS SOLUBILIS 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# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-9233-1 Mercurius Combination9233 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 63083-9233 MERCURIUS COMBINATION 9233 (MERCURIUS COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220210_42e1d05d-c0ab-48f3-94d2-1a1d3e1d2944.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 63083-9233-1 63083923301 29.5 mL in 1 BOTTLE, DROPPER (63083-9233-1) 29.5 ml 1985-08-15 0000-00-00 No No Current