Biotox Para description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Biotox Para

The Wellness Center
Apotheca Company

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

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

Dr. Theresa Dale's

NDC: 50181-0014-1

Bio Tox

Para

1 FL OZ (30 ml)

Biotox Para

Biotox Para

Cochlearia Armoracia, Toxoplasma Gondii, Vibrio Cholerae, Candida Albicans, Trichinella Spiralis LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50181-0014
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
HORSERADISH HORSERADISH 3 [hp_X]
TOXOPLASMA GONDII TOXOPLASMA GONDII 12 [hp_X]
VIBRIO CHOLERAE VIBRIO CHOLERAE 30 [hp_X]
CANDIDA ALBICANS candida albicans 30 [hp_X]
TRICHINELLA SPIRALIS TRICHINELLA SPIRALIS 30 [hp_X]
TARAXACUM OFFICINALE Taraxacum Officinale 8 [hp_C]
PLASMODIUM MALARIAE PLASMODIUM MALARIAE 12 [hp_C]
TRICHOPHYTON RUBRUM Trichophyton rubrum 200 [hp_C]

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL

Packaging

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

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-06-07


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.