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.
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.
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, Coxiella burnetii 60X, 200X, 30C, Francisella tularensis 60X, 30C, Yersinia enterocolitica 60X, 30C, Brucella melitensis 9C, 30C, 60C, Citrobacter diversus 9C, 30C, 60C, Bacillus cereus 12C, Serratia marcescenis 12C, 30C, Enterobacter aerogenes 15C, 30C, 60C, Pestinum 5C, 30C, 60C, 200C, Pseudomonas aeruginosa 60C, Proteus (mirabilis) 30C, 100C, 200C.
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.
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. In case of overdose, get medical help or contact a Poison Control Center right away.
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.
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.
Demineralized Water, 25% Ethanol.
MFD FOR:
The Wellness Center for Research and Education, Inc.
1237 S. Victoria Ave. Suite 169
Oxnard, CA 93035
1-866-962-6484
Dr. Theresa Dale's
NDC: 50181-0045-1
Homeopathic
BioTox Bac I
1 fl oz (30 ml)
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 50181-0045-1 | 2025-06-04 | C162847 | 48780-1 | 9d75b9cf-ee91-f424-e053-dadaa90a57ce | Drug Facts: |
| 50181-0045-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-ee91-f424-e053-dadaa90a57ce | Drug Facts: |
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| BACILLUS ANTHRACIS IMMUNOSERUM RABBIT | ACTIVE INGREDIENT | 41LZ22DD4N | 2 | |
| BACILLUS CEREUS | ACTIVE INGREDIENT | 7YC151N82L | 2 | |
| BRUCELLA ABORTUS | ACTIVE INGREDIENT | 492LCM0TUL | 2 | |
| BRUCELLA MELITENSIS | ACTIVE INGREDIENT | OQF85710LZ | 2 | |
| CITROBACTER KOSERI | ACTIVE INGREDIENT | WP4441Y804 | 2 | |
| CLOSTRIDIUM TETANI | ACTIVE INGREDIENT | 751E8J54VM | 2 | |
| COXIELLA BURNETII | ACTIVE INGREDIENT | GRY5SDU86N | 2 | |
| ENTEROBACTER AEROGENES | ACTIVE INGREDIENT | 2EIQ8686WC | 2 | |
| ESCHERICHIA COLI | ACTIVE INGREDIENT | 514B9K0L10 | 2 | |
| FRANCISELLA TULARENSIS | ACTIVE INGREDIENT | NNR1301B0H | 2 | |
| GERMANIUM | ACTIVE INGREDIENT | 00072J7XWS | 2 | |
| HORSERADISH | ACTIVE INGREDIENT | 8DS6G120HJ | 2 | |
| HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED | ACTIVE INGREDIENT | U364V64HUN | 2 | |
| PROTEUS MIRABILIS | ACTIVE INGREDIENT | C177VR41DV | 2 | |
| PSEUDOMONAS AERUGINOSA | ACTIVE INGREDIENT | Y793W5V55N | 2 | |
| RANCID BEEF | ACTIVE INGREDIENT | 29SUH5R3HU | 2 | |
| SERRATIA MARCESCENS | ACTIVE INGREDIENT | FB3Y68CF2Y | 2 | |
| TABEBUIA IMPETIGINOSA BARK | ACTIVE INGREDIENT | 6GLA1946WX | 2 | |
| TARAXACUM OFFICINALE | ACTIVE INGREDIENT | 39981FM375 | 2 | |
| YERSINIA ENTEROCOLITICA | ACTIVE INGREDIENT | AUL7Y5Z806 | 2 | |
| YERSINIA PESTIS | ACTIVE INGREDIENT | S6JJH3XV1D | 2 | |
| BACILLUS ANTHRACIS IMMUNOSERUM RABBIT | ACTIVE MOIETY | 41LZ22DD4N | 2 | |
| BACILLUS CEREUS | ACTIVE MOIETY | 7YC151N82L | 2 | |
| BRUCELLA ABORTUS | ACTIVE MOIETY | 492LCM0TUL | 2 | |
| BRUCELLA MELITENSIS | ACTIVE MOIETY | OQF85710LZ | 2 | |
| CITROBACTER KOSERI | ACTIVE MOIETY | WP4441Y804 | 2 | |
| CLOSTRIDIUM TETANI | ACTIVE MOIETY | 751E8J54VM | 2 | |
| COXIELLA BURNETII | ACTIVE MOIETY | GRY5SDU86N | 2 | |
| ENTEROBACTER AEROGENES | ACTIVE MOIETY | 2EIQ8686WC | 2 | |
| ESCHERICHIA COLI | ACTIVE MOIETY | 514B9K0L10 | 2 | |
| FRANCISELLA TULARENSIS | ACTIVE MOIETY | NNR1301B0H | 2 | |
| GERMANIUM | ACTIVE MOIETY | 00072J7XWS | 2 | |
| HORSERADISH | ACTIVE MOIETY | 8DS6G120HJ | 2 | |
| HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED | ACTIVE MOIETY | U364V64HUN | 2 | |
| PROTEUS MIRABILIS | ACTIVE MOIETY | C177VR41DV | 2 | |
| PSEUDOMONAS AERUGINOSA | ACTIVE MOIETY | Y793W5V55N | 2 | |
| RANCID BEEF | ACTIVE MOIETY | 29SUH5R3HU | 2 | |
| SERRATIA MARCESCENS | ACTIVE MOIETY | FB3Y68CF2Y | 2 | |
| TABEBUIA IMPETIGINOSA BARK | ACTIVE MOIETY | 6GLA1946WX | 2 | |
| TARAXACUM OFFICINALE | ACTIVE MOIETY | 39981FM375 | 2 | |
| YERSINIA ENTEROCOLITICA | ACTIVE MOIETY | AUL7Y5Z806 | 2 | |
| YERSINIA PESTIS | ACTIVE MOIETY | S6JJH3XV1D | 2 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | 2 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 2 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 50181-0045 | 50181-0045-1 |
Every source-derived ingredient row is available through these pages.
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TOPICAL | 2445 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAMUSCULAR | 1491 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY, METERED / SUBLINGUAL | 29 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / RESPIRATORY (INHALATION) | 35.75 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAMUSCULAR | 1000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TRANSDERMAL | 49.37 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TOPICAL | 3633 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LOTION / TOPICAL | 25 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SHAMPOO / TOPICAL | 714 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TRANSDERMAL | 90 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TRANSDERMAL | 7360 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVENOUS | 99 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / ORAL | 198 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | PASTE / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAVENOUS | 6405 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / SUBCUTANEOUS | 149 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / SUBCUTANEOUS | 6.1 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | POWDER, FOR SOLUTION / TOPICAL | 40 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, FOAM / TOPICAL | 4504 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / RESPIRATORY (INHALATION) | 5 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TOPICAL | 541 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / BUCCAL | 679 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / INTRAVENOUS | 4000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SWAB / TOPICAL | 2250 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | JELLY / VAGINAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / RECTAL | 0.35 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / RESPIRATORY (INHALATION) | 26664 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / DENTAL | 12.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / SUBLINGUAL | 397 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / NASAL | 70 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAVENOUS | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | MOUTHWASH / BUCCAL | 200 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TRANSDERMAL | 3675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / OPHTHALMIC | 0.5 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVESICAL | 7892 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / RESPIRATORY (INHALATION) | 0.08 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAMUSCULAR | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVENOUS | 92 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, EMULSION / INTRAVENOUS | 520 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVASCULAR | 100 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / RECTAL | 898 mg |
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 |
|---|---|---|---|---|---|---|
| 4cdc1a3f-af33-4f48-ac21-a10b56060900 | 08cd89d3-6f52-4d1a-bd13-044a0348a737 | 2025-06-04 | Warnings | 4cdc1a3f-af33-4f48-ac21-a10b56060900 08cd89d3-6f52-4d1a-bd13-044a0348a737 |
Adverse event summaries are temporarily unavailable. Other product information remains available.