FDA.reportPublic FDA data

Bio Biological Detox

Product NDC
43857-0464
Requested package NDC
43857-0464-1
11-digit product format
438570464
Labeler code
43857
Product ID
43857-0464_de7ee970-54c3-44df-a556-d67f86e47067
Type
HUMAN OTC DRUG
Nonproprietary name
Echinacea (Angustifolia), Lomatium Dissectum, Myrrha, Nasturtium Aquaticum, Propolis, Tabebuia Impetiginosa, Hydrastis Canadensis, Thymus Serpyllum, Glandula Suprarenalis Suis, Lymph Node (Suis), Spleen (Suis), Thyroidinum (Suis), Belladonna, Hypericum Perforatum, Phosphorus, Pyrogenium, Anthracinum, Arsenicum Album, Carbolicum Acidum, Hepar Sulphuris Calcareum, Tarentula Cubensis, Variolinum, Botulinum, Bacillus Dysentery, Gaertner Bacillus, Mutabile Bacillus, Francisella Tularensis, Coxiella Burnetii,
Dosage form
SPRAY
Route
ORAL
Labeler
BioActive Nutritional, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2017-11-02
Marketing end
0000-00-00
Substance
ECHINACEA ANGUSTIFOLIA; LOMATIUM DISSECTUM ROOT; MYRRH; NASTURTIUM OFFICINALE; PROPOLIS WAX; TABEBUIA IMPETIGINOSA BARK; GOLDENSEAL; THYMUS SERPYLLUM; SUS SCROFA ADRENAL GLAND; SUS SCROFA LYMPH; SUS SCROFA SPLEEN; SUS SCROFA THYROID; ATROPA BELLADONNA; HYPERICUM PERFORATUM; PHOSPHORUS; RANCID BEEF; BACILLUS ANTHRACIS IMMUNOSERUM RABBIT; ARSENIC TRIOXIDE; PHENOL; CALCIUM SULFIDE; CITHARACANTHUS SPINICRUS; VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN; BOTULINUM TOXIN TYPE A; SHIGELLA DYSENTERIAE; SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS; FRANCISELLA TULARENSIS; COXIELLA BURNETII; CANIS LUPUS FAMILIARIS MILK; PLASMODIUM MALARIAE; ESCHERICHIA COLI; HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED; YERSINIA PESTIS; SULFUR
Active strength
3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/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; [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
2022-12-31
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 packagepackage43857-046443857-0464-1DDiscontinued 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 · 6 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…
2024-05-28 21:12 UTC · source 2024-05-288af77b9d5b6f…d9bbb34c5368…
2024-05-15 03:39 UTC · source 2024-05-14834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-081332a3947898…d4bfe170f9cd…
2020-12-18 03:04 UTC · source 2020-12-17e2bbac7714bc…27bdfed8d636…
2020-06-10 20:45 UTC · source 2020-06-109bebd1f3094a…5416666fcb17…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
2a92e090-adb9-48d2-ae5f-5956e4b6ad90Product name120231024
525448fb-6d30-4c07-bb80-9a8499bd8113Product name120230627
0cf2215a-e8b6-4688-9989-d0fcd154e4b8Product name120170725
8c498f95-3b71-4acf-9882-f567b5cc4a2aProduct name120160208
e9681bd0-ddf1-421f-88c4-4337e89d5421Product name120160208
a42a1284-ee26-4b9f-a2b3-1ba05f250710Product name120151202

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2024-10-02DRUG FACTS:
2024-10-02DRUG FACTS:
2023-01-30DRUG FACTS:
2023-01-30DRUG FACTS:
2021-07-22DRUG FACTS:
2021-07-22DRUG FACTS:
2020-01-31DRUG FACTS:
2020-01-31DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43857-0464-1Bio Biological Detox30 mL in 1 BOTTLE, SPRAYSPRAY305

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43857-0464BIO BIOLOGICAL DETOX (ECHINACEA (ANGUSTIFOLIA), LOMATIUM DISSECTUM, MYRRHA, NASTURTIUM AQUATICUM, PROPOLIS, TABEBUIA IMPETIGINOSA, HYDRASTIS CANADENSIS, THYMUS SERPYLLUM, GLANDULA SUPRARENALIS SUIS, LYMPH NODE (SUIS), SPLEEN (SUIS), THYROIDINUM (SUIS), BELLADONNA, HYPERICUM PERFORATUM, PHOSPHORUS, PYROGENIUM, ANTHRACINUM, ARSENICUM ALBUM, CARBOLICUM ACIDUM, HEPAR SULPHURIS CALCAREUM, TARENTULA CUBENSIS, VARIOLINUM, BOTULINUM, BACILLUS DYSENTERY, GAERTNER BACILLUS, MUTABILE BACILLUS, FRANCISELLA TULARENSIS, COXIELLA BURNETII,) SPRAY [BIOACTIVE NUTRITIONAL, INC.]4Legacy NDC, 1 package rows20241004_f8c42818-7937-4082-bc42-df032cc0ca89.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43857-0464-14385704640130 mL in 1 BOTTLE, SPRAY (43857-0464-1) 30 ml2017-11-020000-00-00NoNoCurrent