BIOTOX

Product NDC
50181-0062
Requested package NDC
50181-0062-1
11-digit product format
501810062
Labeler code
50181
Product ID
50181-0062_e6bad0ca-7902-40f7-96d2-486a8dce415e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Cochlearia Armoracia, Spleen (Bovine), Thymus Gland (Bovine), Influenzinum (2019-2020), Mycoplasma Pneumoniae, Cytomegalovirus Nosode, Human Papilloma Nosode, Coxsackie B1 Nosode, Coxsackie B4 Nosode, Pneumococcinum, Carcinosin
Dosage form
LIQUID
Route
ORAL
Labeler
The Wellness Center for Research and Education, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2020-03-09
Marketing end
0000-00-00
Substance
HORSERADISH; BOS TAURUS SPLEEN; BOS TAURUS THYMUS; INFLUENZA A VIRUS A/BRISBANE/02/2018 IVR-190 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED); INFLUENZA A VIRUS A/KANSAS/14/2017 X-327 (H3N2) ANTIGEN (FORMALDEHYDE INACTIVATED); INFLUENZA B VIRUS B/MARYLAND/15/2016 ANTIGEN (FORMALDEHYDE INACTIVATED); MYCOPLASMA PNEUMONIAE; HUMAN HERPESVIRUS 5; HUMAN PAPILLOMAVIRUS; HUMAN COXSACKIEVIRUS B1; HUMAN COXSACKIEVIRUS B4; STREPTOCOCCUS PNEUMONIAE; HUMAN BREAST TUMOR CELL
Active strength
3 [hp_X]/mL; [hp_X]/mL; 1/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
Pharmacologic classes
Non-Standardized Food Allergenic Extract [EPC],Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Food Additives [CS]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage50181-006250181-0062-1DDiscontinued by firm2026-10-05

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 · 17 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Code, Status table
Captured / source dateCodeStatusSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05DDiscontinued by firmd630ba8d3edf…732f749b63fb…
2025-04-01 02:39 UTC · source 2025-03-31IInactivated by FDA2ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28IInactivated by FDAa1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21IInactivated by FDAcfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10IInactivated by FDAcdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31IInactivated by FDA302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20IInactivated by FDAed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10IInactivated by FDA0efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08IInactivated by FDAad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03IInactivated by FDA367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09IInactivated by FDA557ba5c1ecfa…9c80585c8c6e…
2024-05-28 21:12 UTC · source 2024-05-28IInactivated by FDA8af77b9d5b6f…d9bbb34c5368…
2024-05-15 03:39 UTC · source 2024-05-14IInactivated by FDA834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-08IInactivated by FDA1332a3947898…d4bfe170f9cd…
2022-08-30 03:57 UTC · source 2022-08-29IInactivated by FDAfb8cb913e6d1…eb8c232b6be0…
2022-04-09 23:13 UTC · source 2022-04-08IInactivated by FDA86f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01IInactivated by FDAbd6a592717d7…303034d00443…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50181-0062-12025-06-03C16284748780-1d6a99b39-d46c-a426-e053-dadaa90af4c2DRUG FACTS:
50181-0062-12022-01-28C16284748780-1d6a99b39-d46c-a426-e053-dadaa90af4c2DRUG FACTS:

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50181-0062BIOTOX VI (COCHLEARIA ARMORACIA, SPLEEN (BOVINE), THYMUS GLAND (BOVINE), INFLUENZINUM (2019-2020), MYCOPLASMA PNEUMONIAE, CYTOMEGALOVIRUS NOSODE, HUMAN PAPILLOMA NOSODE, COXSACKIE B1 NOSODE, COXSACKIE B4 NOSODE, PNEUMOCOCCINUM, CARCINOSIN) LIQUID [THE WELLNESS CENTER FOR RESEARCH AND EDUCATION, INC.]1Legacy NDC20200310_5bc05369-ad93-4e91-88bc-aaa6fc7c35ca.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50181-0062-15018100620130 mL in 1 BOTTLE, DROPPER (50181-0062-1) 30 ml2020-03-090000-00-00NoNoCurrent