BioTox Lyme description, usages, side effects, indications, overdosage, supplying and lots more!

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BioTox Lyme

The Wellness Center for Research and Education
Apotheca Company

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENTS:

Phytolacca decandra 6X, Ehrlichia 8X, 15X, 30X, Mycoplasma pneumoniae 9X, 15X, 30X, 200X, 30C, Borrelia burgdorferi 12X, 30X, 60X, 1LM, Babesia microti 15X, 30X, 60X, 5C, Coxiella burnetii 30X, Chelidonium majus 6XC, Herpes zoster 6C, Francisella tularensis 6C, 12C, 30C, Rickettsia rickettsii 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 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:

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

DIRECTIONS:

5 drops 2 or 3 times per day, on an empty stomach, 5 days per week or until symptoms abate.  Consult a physicial 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 50181-0038-1

Homeopathic

BioTox Lyme

1 fl oz (30 ml)

BioTox Lyme

BioTox Lyme

Phytolacca decandra, Ehrlichia, Mycoplasma pneumoniae, Borrelia burgdorferi, Babesia microti, Coxiella burnetii, Chelidonium majus, Herpes zoster, LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50181-0038
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PHYTOLACCA AMERICANA ROOT PHYTOLACCA AMERICANA ROOT 6 [hp_X]
EHRLICHIA CHAFFEENSIS EHRLICHIA CHAFFEENSIS 8 [hp_X]
MYCOPLASMA PNEUMONIAE MYCOPLASMA PNEUMONIAE 9 [hp_X]
BORRELIA BURGDORFERI BORRELIA BURGDORFERI 12 [hp_X]
BABESIA MICROTI BABESIA MICROTI 15 [hp_X]
COXIELLA BURNETII COXIELLA BURNETII 30 [hp_X]
CHELIDONIUM MAJUS CHELIDONIUM MAJUS 6 [hp_C]
HUMAN HERPESVIRUS 3 HUMAN HERPESVIRUS 3 6 [hp_C]
FRANCISELLA TULARENSIS FRANCISELLA TULARENSIS 6 [hp_C]
RICKETTSIA RICKETTSII RICKETTSIA RICKETTSII 7 [hp_C]

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:50181-0038-1 30 in 1 BOTTLE, DROPPER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2014-03-13


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