DailyMed - POLLUTOX- sulphuricum acidum, berberis vulgaris, arsenicum album, benzinum, cadmium sulphuratum, hydrofluoricum acidum, melatonin, nitrogenum oxygenatum, nux vomica, petroleum, plumbum metallicum, stannum metallicum, toluene, acetone, carbon dioxide, chlorinum, mercurius solubilis, uranium nitricum, ozone liquid

NDC Code(s): 43742-2037-1
Packager: Deseret Biologicals, Inc.

Category: HUMAN OTC DRUG LABEL
DEA Schedule: None
Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated October 26, 2023

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ACTIVE INGREDIENTS:
Sulphuricum Acidum 6X, 12X, 30X, Berberis Vulgaris 8X, Arsenicum Album 12X, Benzinum 12X, Cadmium Sulphuratum 12X, Hydrofluoricum Acidum 12X, Melatonin 12X, Nitrogenum Oxygenatum 12X, Nux Vomica ...

Sulphuricum Acidum 6X, 12X, 30X, Berberis Vulgaris 8X, Arsenicum Album 12X, Benzinum 12X, Cadmium Sulphuratum 12X, Hydrofluoricum Acidum 12X, Melatonin 12X, Nitrogenum Oxygenatum 12X, Nux Vomica 12X, Petroleum 12X, Plumbum Metallicum 12X, Stannum Metallicum 12X, Toluene 12X, Acetone 12X, 15X, 30X, Carbon Dioxide 12X, 15X, 30X, Chlorinum 12X, 15, 30, Mercurius Solubilis 12X, 15, 30, Uranium Nitricum 15C, Ozone 16X.
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PURPOSE:
For the temporary relief of symptoms related to pollution such as nausea, fatigue, head discomfort and abdominal discomfort.** **These statements are based upon homeopathic principles. They have ...

For the temporary relief of symptoms related to pollution such as nausea, fatigue, head discomfort and abdominal discomfort.**

**These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
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WARNINGS:
Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use. Tamper Seal ...

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

If pregnant or breast-feeding, ask a health professional before use.

Tamper Seal: "Sealed for Your Protection."

Do not use if seal is broken or missing.
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KEEP OUT OF REACH OF CHILDREN:
In case of overdose, contact a physician or Poison Control Center right away.

In case of overdose, contact a physician or Poison Control Center right away.
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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.

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.
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INDICATIONS:
For the temporary relief of symptoms related to pollution such as nausea, fatigue, head discomfort and abdominal discomfort.** **These statements are based upon homeopathic principles. They have ...

For the temporary relief of symptoms related to pollution such as nausea, fatigue, head discomfort and abdominal discomfort.**

**These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
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INACTIVE INGREDIENTS:
Demineralized Water, 25% Ethanol

Demineralized Water, 25% Ethanol
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QUESTIONS:
Dist. By: Deseret Biologicals, Inc. 469 W. Parkland Drive - Sandy, UT 84070 www.desbio.com

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070 www.desbio.com
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PACKAGE LABEL DISPLAY:
DESBIO - NDC 43742-2037-1 - HOMEOPATHIC - PolluTox - 1 FL OZ (30 ml)

DESBIO
NDC 43742-2037-1
HOMEOPATHIC

PolluTox

1 FL OZ (30 ml)

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INGREDIENTS AND APPEARANCE

Product Information

POLLUTOX sulphuricum acidum, berberis vulgaris, arsenicum album, benzinum, cadmium sulphuratum, hydrofluoricum acidum, melatonin, nitrogenum oxygenatum, nux vomica, petroleum, plumbum metallicum, stannum metallicum, toluene, acetone, carbon dioxide, chlorinum, mercurius solubilis, uranium nitricum, ozone liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:43742-2037
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SULFURIC ACID (UNII: O40UQP6WCF) (SULFURIC ACID - UNII:O40UQP6WCF)	SULFURIC ACID	6 [hp_X] in 1 mL
BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U)	BERBERIS VULGARIS ROOT BARK	8 [hp_X] in 1 mL
ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV)	ARSENIC TRIOXIDE	12 [hp_X] in 1 mL
BENZENE (UNII: J64922108F) (BENZENE - UNII:J64922108F)	BENZENE	12 [hp_X] in 1 mL
CADMIUM SULFIDE (UNII: 057EZR4Z7Q) (CADMIUM CATION - UNII:T494FZ4G8G)	CADMIUM SULFIDE	12 [hp_X] in 1 mL
HYDROFLUORIC ACID (UNII: RGL5YE86CZ) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	12 [hp_X] in 1 mL
MELATONIN (UNII: JL5DK93RCL) (MELATONIN - UNII:JL5DK93RCL)	MELATONIN	12 [hp_X] in 1 mL
NITROUS OXIDE (UNII: K50XQU1029) (NITROUS OXIDE - UNII:K50XQU1029)	NITROUS OXIDE	12 [hp_X] in 1 mL
STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919)	STRYCHNOS NUX-VOMICA SEED	12 [hp_X] in 1 mL
KEROSENE (UNII: 1C89KKC04E) (KEROSENE - UNII:1C89KKC04E)	KEROSENE	12 [hp_X] in 1 mL
LEAD (UNII: 2P299V784P) (LEAD - UNII:2P299V784P)	LEAD	12 [hp_X] in 1 mL
TIN (UNII: 387GMG9FH5) (TIN - UNII:387GMG9FH5)	TIN	12 [hp_X] in 1 mL
TOLUENE (UNII: 3FPU23BG52) (TOLUENE - UNII:3FPU23BG52)	TOLUENE	12 [hp_X] in 1 mL
ACETONE (UNII: 1364PS73AF) (ACETONE - UNII:1364PS73AF)	ACETONE	12 [hp_X] in 1 mL
CARBON DIOXIDE (UNII: 142M471B3J) (CARBON DIOXIDE - UNII:142M471B3J)	CARBON DIOXIDE	12 [hp_X] in 1 mL
CHLORINE (UNII: 4R7X1O2820) (CHLORINE - UNII:4R7X1O2820)	CHLORINE	12 [hp_X] in 1 mL
MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (MERCURIUS SOLUBILIS - UNII:324Y4038G2)	MERCURIUS SOLUBILIS	12 [hp_X] in 1 mL
URANYL NITRATE HEXAHYDRATE (UNII: 3V057702FY) (URANIUM CATION (6+) - UNII:5PI36AS4G7)	URANYL NITRATE HEXAHYDRATE	15 [hp_C] in 1 mL
OZONE (UNII: 66H7ZZK23N) (OZONE - UNII:66H7ZZK23N)	OZONE	16 [hp_X] in 1 mL

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:43742-2037-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	07/21/2023	07/18/2027

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		07/21/2023	07/18/2027

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(43742-2037) , api manufacture(43742-2037) , label(43742-2037) , pack(43742-2037)

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Published Date (What is this?)	Version	Files
Oct 27, 2023	2 (current)	download
Jul 24, 2023	1	download

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