Home NDC 63083-9232-1 Magnesium Combination
Product NDC 63083-9232
Requested package NDC 63083-9232-1
11-digit product format 630839232
Labeler code 63083
Product ID 63083-9232_b72006c9-04da-4aea-aba9-949d15be3b67
Type HUMAN OTC DRUG
Nonproprietary name Magnesium Combination
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance ARTEMISIA ANNUA FLOWERING TOP; PASSIFLORA INCARNATA FLOWERING TOP; AMANITA MUSCARIA FRUITING BODY; AMMONIUM BROMIDE; ACONITUM NAPELLUS WHOLE; ATROPINE SULFATE; CITRULLUS COLOCYNTHIS FRUIT PULP; CUPRIC CATION; GELSEMIUM SEMPERVIRENS ROOT; HYOSCYAMUS NIGER; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; VERATRUM ALBUM ROOT
Active strength 3; 3; 4; 4; 6; 6; 6; 6; 6; 6; 6; 6 [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; [hp_X]/29.5mL
Pharmacologic classes Anticholinergic [EPC], Calculi Dissolution Agent [EPC], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [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 Magnesium Combination
Brand name suffix 9232
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARTEMISIA ANNUA FLOWERING TOP 3 [hp_X]/29.5mL PASSIFLORA INCARNATA FLOWERING TOP 3 [hp_X]/29.5mL AMANITA MUSCARIA FRUITING BODY 4 [hp_X]/29.5mL AMMONIUM BROMIDE 4 [hp_X]/29.5mL ACONITUM NAPELLUS WHOLE 6 [hp_X]/29.5mL ATROPINE SULFATE 6 [hp_X]/29.5mL CITRULLUS COLOCYNTHIS FRUIT PULP 6 [hp_X]/29.5mL CUPRIC CATION 6 [hp_X]/29.5mL GELSEMIUM SEMPERVIRENS ROOT 6 [hp_X]/29.5mL HYOSCYAMUS NIGER 6 [hp_X]/29.5mL MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 6 [hp_X]/29.5mL VERATRUM ALBUM ROOT 6 [hp_X]/29.5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 12 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 R232 2026-01-09 R232 2024-01-30 R232 2024-01-30 R232
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-9232-1 Magnesium Combination9232 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 63083-9232 MAGNESIUM COMBINATION 9232 (MAGNESIUM COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220210_4d99b3ec-724f-4385-ae5e-83389bb0c8fe.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 63083-9232-1 63083923201 29.5 mL in 1 BOTTLE, DROPPER (63083-9232-1) 29.5 ml 1985-08-15 0000-00-00 No No Current