BioTox DIP

Product NDC
50181-0059
Requested package NDC
50181-0059-1
11-digit product format
501810059
Labeler code
50181
Product ID
50181-0059_41964e1b-bfe5-41a7-a0c7-55607148d506
Type
HUMAN OTC DRUG
Nonproprietary name
Aconitum Napellus, Arsenicum Album, Kali Bichromicum, Kali Muriaticum, Kali Phosphoricum, Lachesis Mutus, Lycopodium Clavatum, Mercurius Cyanatus, Phytolacca Decandra, Rhus Tox
Dosage form
LIQUID
Route
ORAL
Labeler
The Wellness Center For Research and Education
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2018-03-16
Marketing end
0000-00-00
Substance
ACONITUM NAPELLUS; ARSENIC TRIOXIDE; POTASSIUM DICHROMATE; POTASSIUM CHLORIDE; DIBASIC POTASSIUM PHOSPHATE; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; MERCURIC CYANIDE; PHYTOLACCA AMERICANA ROOT; TOXICODENDRON PUBESCENS LEAF
Active strength
6 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
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 packagepackage50181-005950181-0059-1DDiscontinued 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 · 2 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage50181-005950181-0059-1DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage50181-005950181-0059-1DDiscontinued by firmexcluded / ndc_excluded.zipf5e01cc5f278…a2eaf40c39c3…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50181-0059BIOTOX DIP (ACONITUM NAPELLUS, ARSENICUM ALBUM, KALI BICHROMICUM, KALI MURIATICUM, KALI PHOSPHORICUM, LACHESIS MUTUS, LYCOPODIUM CLAVATUM, MERCURIUS CYANATUS, PHYTOLACCA DECANDRA, RHUS TOX) LIQUID [THE WELLNESS CENTER FOR RESEARCH AND EDUCATION]1Legacy NDC20180319_d5db8bd2-9ea2-49bf-9b6e-d26d9f841d81.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50181-0059-15018100590130 mL in 1 BOTTLE, DROPPER (50181-0059-1) 30 ml2018-03-160000-00-00NoNoCurrent