Home NDC 63083-4009-2 Mycobacter/Mycoplasma Nosode
Product NDC 63083-4009
Requested package NDC 63083-4009-2
11-digit product format 630834009
Labeler code 63083
Product ID 63083-4009_834af3a3-fb42-4f6d-b8d1-4631c1f8d133
Type HUMAN OTC DRUG
Nonproprietary name Mycobacter/Mycoplasma Nosode
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance ARSENIC TRIIODIDE; BACILLUS ANTHRACIS IMMUNOSERUM RABBIT; MYCOBACTERIUM ABSCESSUS; MYCOBACTERIUM AVIUM; MYCOBACTERIUM AVIUM SUBSP. PARATUBERCULOSIS; MYCOPLASMA PNEUMONIAE; STRYCHNOS NUX-VOMICA SEED; SULFUR; SULFURIC ACID
Active strength 30; 30; 30; 30; 30; 30; 100; 100; 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
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
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 Mycobacter/Mycoplasma Nosode
Brand name suffix 4009
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARSENIC TRIIODIDE 30 [hp_X]/59mL SULFURIC ACID 30 [hp_X]/59mL STRYCHNOS NUX-VOMICA SEED 100 [hp_X]/59mL SULFUR 100 [hp_X]/59mL BACILLUS ANTHRACIS IMMUNOSERUM RABBIT 30 [hp_X]/59mL MYCOBACTERIUM ABSCESSUS 30 [hp_X]/59mL MYCOBACTERIUM AVIUM 30 [hp_X]/59mL MYCOBACTERIUM AVIUM SUBSP. PARATUBERCULOSIS 30 [hp_X]/59mL MYCOPLASMA PNEUMONIAE 30 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 9 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 N9 2026-01-09 N9 2024-01-30 N9 2024-01-30 N9
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-4009-2 Mycobacter/Mycoplasma Nosode4009 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 63083-4009 MYCOBACTER/MYCOPLASMA NOSODE 4009 (MYCOBACTER/MYCOPLASMA NOSODE) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220301_157e22fa-0791-4e8b-9d3a-7b6e94882c66.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 63083-4009-2 63083400902 59 mL in 1 BOTTLE, DROPPER (63083-4009-2) 59 ml 1985-08-15 0000-00-00 No No Current