Borrelia Babesia Remedy description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Borrelia Babesia Remedy

Deseret Biologicals, Inc.
Apotheca Company

DRUG FACTS:


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENTS:

Babesia Microti 15X, Borrelia Burgdorferi 15X, 20X, 30X, 60X, 90X, 120X, 150X, 200X, 500X, 1000X

INDICATIONS:

For the temporary relief of symptoms related to Lyme Disease including rash, fever, chills, fatigue, migratory joint pain, memory loss, sleep disorders and rapid heart beat.

WARNINGS:

​Keep out of reach of children. ​In case of overdose, contact physician or Poison Control Center right away.

​If pregnant or breast-feeding,​ seek advice of a health professional before use.

Tamper seal: "Sealed for Your Protection."

Do not use if seal is broken or missing.

DIRECTIONS:

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

INACTIVE INGREDIENTS:

Demineralized Water, 25% Ethanol

KEEP OUT OF REACH OF CHILDREN.

​Keep out of reach of children.​ In case of overdose, contact physician or Poison Control Center right away.

INDICATIONS:

For the temporary relief of symptoms related to Lyme Disease including rash, fever, chills, fatigue, migratory joint pain, memory loss, sleep disorders and rapid heart beat.

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070

www.desbio.com

PACKAGE DISPLAY LABEL:

DESBIO

NDC 43742-0246-1

HOMEOPATHIC

BORRELIA-BABESIA REMEDY

1 FL OZ (30 mL)

Borrelia Babesia Remedy

Borrelia Babesia Remedy

Babesia Microti, Borrelia Burgdorferi LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:43742-0246
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BABESIA MICROTI BABESIA MICROTI 15 [hp_X]
BORRELIA BURGDORFERI BORRELIA BURGDORFERI 15 [hp_X]

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43742-0246-1 30 in 1 BOTTLE, DROPPER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-08-20


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.