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.
Biotox Lyme
- Manufacturer
- The Wellness Center for Research and Education, Inc. | Apotheca Company
- Effective date
- 2025-05-30
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 20:37:24
Label at a glance#
ProductBiotox Lyme
Active ingredientPHYTOLACCA AMERICANA ROOT, MYCOPLASMA PNEUMONIAE, BORRELIA BURGDORFERI, EHRLICHIA CANIS, BABESIA MICROTI, COXIELLA BURNETII, CHELIDONIUM MAJUS, HUMAN HERPESVIRUS 3, FRANCISELLA TULARENSIS, RICKETTSIA PROWAZEKII
Label structure9 sections
Contacts and useful links#
Label contents#
Full prescribing information#
ACTIVE INGREDIENTS:
Phytolacca Decandra 6X, Mycoplasma Pneumoniae 9X, 15X, 30X, 200X, 30C, Borrelia Burgdorferi Nosode 12X, 30X, 60X, 1LM, Ehrlichia Nosode (Canine) 15X, 30X, , Babesia Microti 15X, 30X, 60X, 5C, Coxiella Burnetii 30X, Chelidonium Majus 6C, Herpes Zoster Nosode 6C, Francisella Tularensis 6C, 12C, 30C, Rickettsia Prowazekii 7C, 15C, 30C.
INDICATIONS:
Chronic fatigue, rash, flu-like symptoms, swelling and joint pain (like arthritis), tingling and numbness in your hands, feet and back, brain fog, poor memory, weakness or paralysis in your face muscles.
WARNINGS:
If pregnant or breastfeeding, 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:
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
DIRECTIONS:
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:
Chronic fatigue, rash, flu-like symptoms, swelling and joint pain (like arthritis), tingling and numbness in your hands, feet and back, brain fog, poor memory, weakness or paralysis in your face muscles.
INACTIVE INGREDIENTS:
Demineralized Water, 25% Ethanol.
QUESTIONS:
MFD FOR:
The Wellness Center for Research
and Education, Inc.
1237 S. Victoria Ave. Suite 169
Oxnard, CA 93035 1-866-962-6484
PACKAGE LABEL DISPLAY:
Dr. Theresa Dale's
NDC: 50181-0056-1
Homeopathic
BioTox Lyme
1 fl oz (30 ml)
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 50181-0056-1 | 2025-05-30 | C162847 | 48780-1 | 9d75b9d1-26df-f424-e053-dadaa90a57ce | Drug Facts: |
| 50181-0056-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-26df-f424-e053-dadaa90a57ce | Drug Facts: |
Products#
Every source-derived product name is available through these pages.
- Biotox Lyme
- Phytolacca Decandra, Mycoplasma Pneumoniae, Borrelia Burgdorferi Nosode, Ehrlichia Nosode (Canine), Babesia Microti, Coxiella Burnetii, Chelidonium Majus, Herpes Zoster Nosode, Francisella Tularensis, Rickettsia Prowazekii
- PHYTOLACCA AMERICANA ROOT
- MYCOPLASMA PNEUMONIAE
- BORRELIA BURGDORFERI
- EHRLICHIA CANIS
- BABESIA MICROTI
- COXIELLA BURNETII
- CHELIDONIUM MAJUS
- HUMAN HERPESVIRUS 3
- FRANCISELLA TULARENSIS
- RICKETTSIA PROWAZEKII
- WATER
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 50181-0056 | 50181-0056-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| PHYTOLACCA AMERICANA ROOT | 11E6VI8VEG | ACTIB |
| MYCOPLASMA PNEUMONIAE | JQE470FAD0 | ACTIB |
| BORRELIA BURGDORFERI | 0J8NV9V5Q8 | ACTIB |
| EHRLICHIA CANIS | 970Y8T1JZY | ACTIB |
| BABESIA MICROTI | 1948X6KEG3 | ACTIB |
| COXIELLA BURNETII | GRY5SDU86N | ACTIB |
| CHELIDONIUM MAJUS | 7E889U5RNN | ACTIB |
| HUMAN HERPESVIRUS 3 | 9885M7D6JP | ACTIB |
| FRANCISELLA TULARENSIS | NNR1301B0H | ACTIB |
| RICKETTSIA PROWAZEKII | TVS414L9M5 | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| e8e6871d-4313-4bde-a72f-2594c256d027 | 8f45fa94-a94a-433c-a13e-9e815b49cb1c | 2025-05-30 | Warnings | e8e6871d-4313-4bde-a72f-2594c256d027 8f45fa94-a94a-433c-a13e-9e815b49cb1c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.