TOXAGENT DETOX 6035- toxagent detox liquid

Toxagent Detox by

Drug Labeling and Warnings

Toxagent Detox by is a Homeopathic medication manufactured, distributed, or labeled by Professional Complementary Health Formulas, Natural Pharmaceutical Manufacturing LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Chlorinum 12X
Chloroformum 12X
Fluorine 12X
Methane 12X
Phospholan 12X
Sulphur amine 12X
Apis mellifica 12X, 30X, 60X
Allium cepa 30X
Ammonium nitricum 30X
Arsenicum album 30X
Caladium seguinum 30X
Nitricum acidum 30X
PCBs 30X
Propane 30X
Sulphuricum acidum 30X
Veratrum album 30X
Calendula officinalis 30X, 60X, 100X
Dioxin 60X
Aconitum napellus 200X
Arnica montana 200X
Benzinum 200X
Hydrocyanicum acidum 200X
Kali cyanatum 200X

QUESTIONS

Professional Formulas

PO Box 2034 Lake Oswego, OR 97035

INDICATIONS

For the temporary relief of irritation of the nose, throat, eyes, or skin, occasional headache, shortness of breath, or fatigue due to sensitivity to or exposure to industrial processes or environmental contaminants.*

PURPOSE

*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS

In case of overdose, get medical help or contact a poison control center right away.

Keep out of the reach of children.

If pregnant or breastfeeding, ask a healthcare professional before use.

DIRECTIONS

Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 drops up to 3 times per day. Consult a physician for use in children under 12 years of age.

OTHER INFORMATION

Tamper resistant. If seal is broken, do not use. After opening, close container tightly and store at room temperature away from heat.

INACTIVE INGREDIENTS

20% ethanol, purified water.

LABEL

Est 1985

Professional Formulas

Complementary Health

Toxagent Detox

Homeopathic Remedy

2 FL. OZ. (59 mL)

INGREDIENTS AND APPEARANCE

TOXAGENT DETOX  6035
toxagent detox liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63083-6035
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLORINE (UNII: 4R7X1O2820) (CHLORINE - UNII:4R7X1O2820)	CHLORINE	12 [hp_X]  in 59 mL
CHLOROFORM (UNII: 7V31YC746X) (CHLOROFORM - UNII:7V31YC746X)	CHLOROFORM	12 [hp_X]  in 59 mL
FLUORINE (UNII: 284SYP0193) (FLUORINE - UNII:284SYP0193)	FLUORINE	12 [hp_X]  in 59 mL
METHANE (UNII: OP0UW79H66) (METHANE - UNII:OP0UW79H66)	METHANE	12 [hp_X]  in 59 mL
PHOSFOLAN (UNII: CHJ98J84AY) (PHOSFOLAN - UNII:CHJ98J84AY)	PHOSFOLAN	12 [hp_X]  in 59 mL
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	12 [hp_X]  in 59 mL
APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z)	APIS MELLIFERA	12 [hp_X]  in 59 mL
ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H)	ONION	30 [hp_X]  in 59 mL
AMMONIUM CATION (UNII: 54S68520I4) (AMMONIUM CATION - UNII:54S68520I4)	AMMONIUM CATION	30 [hp_X]  in 59 mL
ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV)	ARSENIC TRIOXIDE	30 [hp_X]  in 59 mL
DIEFFENBACHIA SEGUINE WHOLE (UNII: 01800C6E6B) (DIEFFENBACHIA SEGUINE WHOLE - UNII:01800C6E6B)	DIEFFENBACHIA SEGUINE WHOLE	30 [hp_X]  in 59 mL
NITRIC ACID (UNII: 411VRN1TV4) (NITRIC ACID - UNII:411VRN1TV4)	NITRIC ACID	30 [hp_X]  in 59 mL
FENSON (UNII: DFC2HB4I0K) (FENSON - UNII:DFC2HB4I0K)	FENSON	30 [hp_X]  in 59 mL
PROPANE (UNII: T75W9911L6) (PROPANE - UNII:T75W9911L6)	PROPANE	30 [hp_X]  in 59 mL
SULFURIC ACID (UNII: O40UQP6WCF) (SULFURIC ACID - UNII:O40UQP6WCF)	SULFURIC ACID	30 [hp_X]  in 59 mL
VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (VERATRUM ALBUM ROOT - UNII:QNS6W5US1Z)	VERATRUM ALBUM ROOT	30 [hp_X]  in 59 mL
CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (CALENDULA OFFICINALIS FLOWERING TOP - UNII:18E7415PXQ)	CALENDULA OFFICINALIS FLOWERING TOP	30 [hp_X]  in 59 mL
2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN (UNII: DO80M48B6O) (2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN - UNII:DO80M48B6O)	2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN	60 [hp_X]  in 59 mL
ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD) (ACONITUM NAPELLUS WHOLE - UNII:U0NQ8555JD)	ACONITUM NAPELLUS WHOLE	200 [hp_X]  in 59 mL
ARNICA MONTANA WHOLE (UNII: O80TY208ZW) (ARNICA MONTANA WHOLE - UNII:O80TY208ZW)	ARNICA MONTANA WHOLE	200 [hp_X]  in 59 mL
BENZENE (UNII: J64922108F) (BENZENE - UNII:J64922108F)	BENZENE	200 [hp_X]  in 59 mL
HYDROGEN CYANIDE (UNII: 2WTB3V159F) (HYDROGEN CYANIDE - UNII:2WTB3V159F)	HYDROGEN CYANIDE	200 [hp_X]  in 59 mL
POTASSIUM CYANIDE (UNII: MQD255M2ZO) (POTASSIUM CATION - UNII:295O53K152)	POTASSIUM CYANIDE	200 [hp_X]  in 59 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63083-6035-2	59 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	08/15/1985

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		08/15/1984

Labeler - Professional Complementary Health Formulas (167339027)

Registrant - Natural Pharmaceutical Manufacturing LLC (015624923)

Establishment
Name	Address	ID/FEI	Business Operations
Natural Pharmaceutical Manufacturing LLC		015624923	manufacture(63083-6035)