BioTox Bac

Manufacturer
The Wellness Center for Research | Apotheca Company
Effective date
2025-06-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:33:57

Label at a glance#

ProductBioTox Bac I
Active ingredientHORSERADISH, TARAXACUM OFFICINALE, TABEBUIA IMPETIGINOSA BARK, BRUCELLA ABORTUS, ESCHERICHIA COLI, GERMANIUM, HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED, BACILLUS ANTHRACIS IMMUNOSERUM RABBIT, CLOSTRIDIUM TETANI, RANCID BEEF, FRANCISELLA TULARENSIS, YERSINIA ENTEROCOLITICA, BRUCELLA MELITENSIS, SERRATIA MARCESCENS, CITROBACTER KOSERI, ENTEROBACTER AEROGENES, YERSINIA PESTIS, BACILLUS CEREUS, PSEUDOMONAS AERUGINOSA, COXIELLA BURNETII, PROTEUS MIRABILIS
Label structure9 sections

Dosage and administration

5 drops orally 2 or 3 times per day, on an empty stomach, 5 days per week or until symptoms abate. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Cochlearia Armoracia 3X, Taraxacum Officinale 3X, Tabebuia Impetiginosa 3X, 6X, 15X, Brucella Abortus 12X, 15X, 30X, 60X, Colibacillinum Cum Natrum Muriaticum 12X, 30X, Germanium 15X, 30X, 60X, Pertussinum 30X, Anthracinum 60X, 200X, 400X, Bacillus Tetani 60X, 200X, 400X, Pyrogenium 60X, 200X, 400X, 30C, Francisella Tularensis 60X, 30C, Yersinia Enterocolitica 60X, 30C, Brucella Melitensis 9C, 30C, 60C, Serratia Marcescenis 12C, 30C, Citrobacter Diversus 12C, 30C, 60C, Enterobacter Aerogenes 15C, 30C, 60C, Pestinum 15C, 30C, 60C, 200C, Bacillus Cereus 18C, Pseudomonas Aeruginosa 30C, 60C, Coxiella Burnetii 30C, 60C, 200C, Proteus (Mirabilis) 30C, 100C, 200C.

INDICATIONS:

OTC - PURPOSE SECTION

Tired, rash, flu-like symptoms, swelling, joint pain, tingling, numbness in your hands, feet or back, brain fog, poor memory, weakness or paralysis in facial muscles.

WARINGS:

WARNINGS SECTION

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if tamper evident seal is broken or missing.

Store in a cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

5 drops orally 2 or 3 times per day, on an empty stomach, 5 days per week or until symptoms abate. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

Tired, rash, flu-like symptoms, swelling, joint pain, tingling, numbness in your hands, feet or back, brain fog, poor memory, weakness or paralysis in facial muscles.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Organic Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

MFD FOR:

The Wellness Center for Research and Education, Inc.

1237 S. Victoria Ave. Suite 169

Oxnard, CA 93035

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dr. Theresa Dale's

NDC: 50181-0075-1

Homeopathic

BioTox Bac I

1 fl oz (30 ml)

BioTox Bac 1BioTox Bac 1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50181-0075-12025-06-06C16284748780-1f386c64a-3807-0266-e053-dadaa90a7c1aDRUG FACTS:
50181-0075-12023-01-30C16284748780-1f386c64a-3807-0266-e053-dadaa90a7c1aDRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50181-0075-1BioTox BacI30 mL in 1 BOTTLE, DROPPERLIQUID302

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50181-007550181-0075-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Source Document#

Source XML

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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
7bc9f839-9052-4213-9923-f810041d30fadf12608a-d29e-4c95-ac06-bbf2c38ba0072025-06-06WarningsExact identifier
spl id: 7bc9f839-9052-4213-9923-f810041d30fa
spl set id: df12608a-d29e-4c95-ac06-bbf2c38ba007

Reported adverse events (FAERS/openFDA)#

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