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Oratox

Deseret Biologicals, Inc.
Apotheca Company

Drug Facts




FULL PRESCRIBING INFORMATION

Fucus Vesiculosus 3X, Lymph node (Suis) 8X, Medulla Ossis Suis 8X, Thymus (Suis) 8X, Thyroidinum (Suis) 8X, Calcarea Muriatica 12X, Iodium 12X, Natrum Fluoratum 12X, Natrum Muriaticum 12X, Selenium Metallicum 12X, Vanadium Metallicum 12X, Argentum metallicum 12X, 30X, 60X, 200X, Aurum metallicum 12X, 30X, 60X, 200X, Cuprum metallicum 12X, 30X, 60X, 200X, Eugenol 12X, 30X, 60X, 200X, Formalinum 12X, 30X, 60X, 200X, Lidocaine 12X, 30X, 60X, 200X, Mercurius solubilis 12X, 30X, 60X, 200X, Molybdenum metallicum 12X, 30X, 60X, 200X, Niccolum metallicum 12X, 30X, 60X, 200X, Palladium metallicum 12X, 30X, 60X, 200X, Stannum metallicum 12X, 30X, 60X, 200X, Titanium metallicum 12X, 30X, 60X, 200X, Zincum Metallicum 12X, 30X, 60X, 200X.

For temporary relief of symptoms related to heavy metal toxicity caused by toxic dental materials in the mouth. These include muscle cramps, ulcerations, inflammation, mental confusion and joint pain.

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.

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.

Demineralized water, 25% Ethanol.

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

For temporary relief of symptoms related to heavy metal toxicity caused by toxic dental materials in the mouth. These include muscle cramps, ulcerations, inflammation, mental confusion and joint pain.

Dist. By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070

www.desbio.com

DESBIO

NDC 43742-0170-1

HOMEOPATHIC

ORATOX

1 FL OZ (30 ml)

Oratox

Oratox

Fucus Vesiculosus, Lymph Node, Medula Ossis Suis, Thymus, Thyroidinum, Calcarea Muriatica, Iodium LIQUID

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:43742-0170
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
FUCUS VESICULOSUS FUCUS VESICULOSUS 3 [hp_X]
SUS SCROFA LYMPH SUS SCROFA LYMPH 8 [hp_X]
SUS SCROFA BONE MARROW SUS SCROFA BONE MARROW 8 [hp_X]
SUS SCROFA THYMUS SUS SCROFA THYMUS 8 [hp_X]
SUS SCROFA THYROID SUS SCROFA THYROID 8 [hp_X]
calcium chloride 12 [hp_X]
Iodine IODINE 12 [hp_X]
SODIUM FLUORIDE FLUORIDE ION 12 [hp_X]
SODIUM CHLORIDE 12 [hp_X]
Selenium SELENIUM 12 [hp_X]
VANADIUM VANADIUM 12 [hp_X]
SILVER Silver 12 [hp_X]
GOLD 12 [hp_X]
Copper COPPER 12 [hp_X]
Eugenol 12 [hp_X]
FORMALDEHYDE FORMALDEHYDE 12 [hp_X]
LIDOCAINE LIDOCAINE 12 [hp_X]
MERCURIUS SOLUBILIS MERCURIUS SOLUBILIS 12 [hp_X]
MOLYBDENUM MOLYBDENUM 12 [hp_X]
NICKEL Nickel 12 [hp_X]
PALLADIUM PALLADIUM 12 [hp_X]
tin Tin 12 [hp_X]
TITANIUM Titanium 12 [hp_X]
Zinc ZINC 12 [hp_X]

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43742-0170-1 30 in 1 BOTTLE, DROPPER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2012-10-31


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