BIOTOX PARA- cochlearia armoracia, toxoplasma gondii, vibrio cholerae, candida albicans, trichinella spiralis liquid

Biotox Para by

Drug Labeling and Warnings

Biotox Para by is a Homeopathic medication manufactured, distributed, or labeled by The Wellness Center, Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Cochlearia Armoracia 3X, Toxoplasma Gondii 12X, 15X, 30X, 60X, 100X, 200X, Vibrio Cholerae 30X, 200X, 400X, Candida Albicans 30X, 200X, 8C, Trichinella Spiralis 30X, 200X, 8C, Cholera 8C, Taraxacum Officinale 8C, Malaria Officinalis 12C, 30C, 60C, 200C, 3LM, Tinea 200C

INDICATIONS

Allergies, distention of abdomen, edema, constipation, diarrhea, intestinal dysbiosis, flu-like symptoms, skin rash, ulcers, boils, fever, vomiting, immune system, intestinal hemorrhaging. 

WARNINGS

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 cool, dry place.

DIRECTIONS

5 drops 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. 

INACTIVE INGREDIENTS

Demineralized Water, 25% Ethanol

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS AND USAGE

Allergies, distention of abdomen, edema, constipation, diarrhea, intestinal dysbiosis, flu-like symptoms, skin rash, ulcers, boils, fever, vomiting, immune system, intestinal hemorrhaging.

QUESTIONS

MFD FOR:

The Wellness Center for

Research and Education, Inc.

1237 S. Victoria Ave. Suite 169

Oxnard, CA 93035

1-866-962-6484

PRINCIPAL DISPLAY PANEL

Dr. Theresa Dale's

NDC: 50181-0014-1

Bio Tox

Para

1 FL OZ (30 ml)

INGREDIENTS AND APPEARANCE

BIOTOX PARA 
cochlearia armoracia, toxoplasma gondii, vibrio cholerae, candida albicans, trichinella spiralis liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50181-0014
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HORSERADISH (UNII: 8DS6G120HJ) (HORSERADISH - UNII:8DS6G120HJ)	HORSERADISH	3 [hp_X]  in 1 mL
TOXOPLASMA GONDII (UNII: BMV90JF469) (TOXOPLASMA GONDII - UNII:BMV90JF469)	TOXOPLASMA GONDII	12 [hp_X]  in 1 mL
VIBRIO CHOLERAE (UNII: 4M0784008H) (VIBRIO CHOLERAE - UNII:4M0784008H)	VIBRIO CHOLERAE	30 [hp_X]  in 1 mL
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	30 [hp_X]  in 1 mL
TRICHINELLA SPIRALIS (UNII: 2PYI6D7HCQ) (TRICHINELLA SPIRALIS - UNII:2PYI6D7HCQ)	TRICHINELLA SPIRALIS	30 [hp_X]  in 1 mL
TARAXACUM OFFICINALE (UNII: 39981FM375) (TARAXACUM OFFICINALE - UNII:39981FM375)	TARAXACUM OFFICINALE	8 [hp_C]  in 1 mL
PLASMODIUM MALARIAE (UNII: AR76CST9I2) (PLASMODIUM MALARIAE - UNII:AR76CST9I2)	PLASMODIUM MALARIAE	12 [hp_C]  in 1 mL
TRICHOPHYTON RUBRUM (UNII: 2ZAU32517N) (TRICHOPHYTON RUBRUM - UNII:2ZAU32517N)	TRICHOPHYTON RUBRUM	200 [hp_C]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50181-0014-1	30 mL in 1 BOTTLE, DROPPER

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		06/07/2013

Labeler - The Wellness Center (832363993)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	api manufacture(50181-0014) , label(50181-0014) , manufacture(50181-0014) , pack(50181-0014)