Home NDC 63083-6013-2 Metex
Product NDC 63083-6013
Requested package NDC 63083-6013-2
11-digit product format 630836013
Labeler code 63083
Product ID 63083-6013_0d802602-9503-40a2-8191-c6d08c514b00
Type HUMAN OTC DRUG
Nonproprietary name Metex
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance PLANTAGO MAJOR WHOLE; COPPER; LYCOPODIUM CLAVATUM SPORE; ALUMINUM OXIDE; ARSENIC TRIOXIDE; CADMIUM; MERCURIUS SOLUBILIS; NICKEL SULFATE HEXAHYDRATE; LEAD; RUBIDIUM; STAINLESS STEEL 316L; TITANIUM
Active strength 3; 6; 6; 30; 30; 30; 30; 30; 30; 30; 30; 30 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Inhibit Ovum Fertilization [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 Metex
Brand name suffix 6013
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PLANTAGO MAJOR WHOLE 3 [hp_X]/59mL COPPER 6 [hp_X]/59mL LYCOPODIUM CLAVATUM SPORE 6 [hp_X]/59mL ALUMINUM OXIDE 30 [hp_X]/59mL ARSENIC TRIOXIDE 30 [hp_X]/59mL CADMIUM 30 [hp_X]/59mL MERCURIUS SOLUBILIS 30 [hp_X]/59mL NICKEL SULFATE HEXAHYDRATE 30 [hp_X]/59mL LEAD 30 [hp_X]/59mL RUBIDIUM 30 [hp_X]/59mL STAINLESS STEEL 316L 30 [hp_X]/59mL TITANIUM 30 [hp_X]/59mL
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 2026-01-08 X13 2026-01-08 X13 2024-01-30 X13 2024-01-30 X13
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-6013-2 Metex6013 59 mL in 1 BOTTLE, DROPPER LIQUID 59 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63083-6013 METEX 6013 (METEX) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220405_78371ca3-50a6-46f0-8ea6-7de57c516375.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 63083-6013-2 63083601302 59 mL in 1 BOTTLE, DROPPER (63083-6013-2) 59 ml 1985-08-15 0000-00-00 No No Current