ORATOX- fucus vesiculosus, lymph node, medulla ossis suis, thymus, thyroidinum, calcarea muriatica, iodium, natrum fluoratum, natrum muriaticum, selenium metallicum, vanadium metallicum, argentum metallicum, aurum metallicum, cuprum metallicum, eugenol, formalinum, lidocaine, mercurius solubilis, molybdenum metallicum, niccolum metallicum, palladium metallicum, stannum metallicum, titanium metallicum, zincum metallicum, liquid

Oratox by

Drug Labeling and Warnings

Oratox by is a Homeopathic medication manufactured, distributed, or labeled by Deseret Biologicals, Inc., Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

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.

HOMEOPATHIC INDICATIONS:

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.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

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, get medical help or contact a Poison Control Center right away.

HOMEOPATHIC INDICATIONS:

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.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

QUESTIONS

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070

www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO

NDC: 43742-0170-1

HOMEOPATHIC

ORATOX

1 FL OZ (30 ml)

INGREDIENTS AND APPEARANCE

ORATOX 
fucus vesiculosus, lymph node, medulla ossis suis, thymus, thyroidinum, calcarea muriatica, iodium, natrum fluoratum, natrum muriaticum, selenium metallicum, vanadium metallicum, argentum metallicum, aurum metallicum, cuprum metallicum, eugenol, formalinum, lidocaine, mercurius solubilis, molybdenum metallicum, niccolum metallicum, palladium metallicum, stannum metallicum, titanium metallicum, zincum metallicum, liquid

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 43742-0170
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FUCUS VESICULOSUS (UNII: 535G2ABX9M) (FUCUS VESICULOSUS - UNII:535G2ABX9M)	FUCUS VESICULOSUS	3 [hp_X]  in 1 mL
SUS SCROFA LYMPH (UNII: 33A7VYU29L) (SUS SCROFA LYMPH - UNII:33A7VYU29L)	SUS SCROFA LYMPH	8 [hp_X]  in 1 mL
SUS SCROFA BONE MARROW (UNII: VP2CN2G7Y8) (SUS SCROFA BONE MARROW - UNII:VP2CN2G7Y8)	SUS SCROFA BONE MARROW	8 [hp_X]  in 1 mL
SUS SCROFA THYMUS (UNII: 7B69B0BD62) (SUS SCROFA THYMUS - UNII:7B69B0BD62)	SUS SCROFA THYMUS	8 [hp_X]  in 1 mL
SUS SCROFA THYROID (UNII: 6RV024OAUQ) (SUS SCROFA THYROID - UNII:6RV024OAUQ)	SUS SCROFA THYROID	8 [hp_X]  in 1 mL
CALCIUM CHLORIDE (UNII: M4I0D6VV5M) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CHLORIDE	12 [hp_X]  in 1 mL
IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4)	IODINE	12 [hp_X]  in 1 mL
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	12 [hp_X]  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CHLORIDE	12 [hp_X]  in 1 mL
SELENIUM (UNII: H6241UJ22B) (SELENIUM - UNII:H6241UJ22B)	SELENIUM	12 [hp_X]  in 1 mL
VANADIUM (UNII: 00J9J9XKDE) (VANADIUM - UNII:00J9J9XKDE)	VANADIUM	12 [hp_X]  in 1 mL
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)	SILVER	12 [hp_X]  in 1 mL
GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO)	GOLD	12 [hp_X]  in 1 mL
COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5)	COPPER	12 [hp_X]  in 1 mL
EUGENOL (UNII: 3T8H1794QW) (EUGENOL - UNII:3T8H1794QW)	EUGENOL	12 [hp_X]  in 1 mL
FORMALDEHYDE (UNII: 1HG84L3525) (FORMALDEHYDE - UNII:1HG84L3525)	FORMALDEHYDE	12 [hp_X]  in 1 mL
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	12 [hp_X]  in 1 mL
MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (MERCURIC CATION - UNII:ED30FJ8Y42)	MERCURIUS SOLUBILIS	12 [hp_X]  in 1 mL
MOLYBDENUM (UNII: 81AH48963U) (MOLYBDENUM - UNII:81AH48963U)	MOLYBDENUM	12 [hp_X]  in 1 mL
NICKEL (UNII: 7OV03QG267) (NICKEL - UNII:7OV03QG267)	NICKEL	12 [hp_X]  in 1 mL
PALLADIUM (UNII: 5TWQ1V240M) (PALLADIUM - UNII:5TWQ1V240M)	PALLADIUM	12 [hp_X]  in 1 mL
TIN (UNII: 387GMG9FH5) (TIN - UNII:387GMG9FH5)	TIN	12 [hp_X]  in 1 mL
TITANIUM (UNII: D1JT611TNE) (TITANIUM - UNII:D1JT611TNE)	TITANIUM	12 [hp_X]  in 1 mL
ZINC (UNII: J41CSQ7QDS) (ZINC - UNII:J41CSQ7QDS)	ZINC	12 [hp_X]  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: 43742-0170-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	10/31/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		10/31/2012	12/02/2020

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(43742-0170) , api manufacture(43742-0170) , label(43742-0170) , pack(43742-0170)