Label: ALLER DETOX OUTDOOR POLLUTION CONTROL- benzinum, calcarea carbonica, carbo vegetabilis, carboneum oxygenisatum, chlorinum, chloroforum, chromium oxydatum, formalinum, hekla lava, hydrastis canadensis, lycopodium clavatum, manganum aceticum, manganum carbonicum, mercurius vivus, nitricum acidum, phosphoricum acidum, phytolacca decandra, plumbum iodatum, plumbum metallicum, sulphur, taraxacum liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 57955-2404-2 - Packager: King Bio 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 June 16, 2015
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ACTIVE INGREDIENT
Drug Facts__________________________________________________________________________________________________________
HPUS active ingredients: Benzinum, Calcarea carbonica, Carbo vegetabilis, Carboneum oxygenisatum, Chlorinum, Chloroformum, Chromium oxydatum, Formalinum, Hekla lava, Hydrastis canadensis, Lycopodium clavatum, Manganum aceticum, Manganum carbonicum, Mercurius vivus, Nitricum acidum, Phosphoricum acidum, Phytolacca decandra, Plumbum iodatum, Plumbum metallicum, Sulphur, Taraxacum. Equal volumes of each ingredient in 12X, 24X, 30C, LM1, LM2, LM3, LM5 potencies.
- INDICATIONS & USAGE
- INACTIVE INGREDIENT
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
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- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ALLER DETOX OUTDOOR POLLUTION CONTROL
benzinum, calcarea carbonica, carbo vegetabilis, carboneum oxygenisatum, chlorinum, chloroforum, chromium oxydatum, formalinum, hekla lava, hydrastis canadensis, lycopodium clavatum, manganum aceticum, manganum carbonicum, mercurius vivus, nitricum acidum, phosphoricum acidum, phytolacca decandra, plumbum iodatum, plumbum metallicum, sulphur, taraxacum liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57955-2404 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZENE (UNII: J64922108F) (BENZENE - UNII:J64922108F) BENZENE 12 [hp_X] in 59 mL OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X] in 59 mL ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL 12 [hp_X] in 59 mL CARBON MONOXIDE (UNII: 7U1EE4V452) (CARBON MONOXIDE - UNII:7U1EE4V452) CARBON MONOXIDE 12 [hp_X] in 59 mL 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 CHROMIC OXIDE (UNII: X5Z09SU859) (CHROMIC OXIDE - UNII:X5Z09SU859) CHROMIC OXIDE 12 [hp_X] in 59 mL FORMALDEHYDE (UNII: 1HG84L3525) (FORMALDEHYDE - UNII:1HG84L3525) FORMALDEHYDE 12 [hp_X] in 59 mL HEKLA LAVA (UNII: C21158IIRK) (HEKLA LAVA - UNII:C21158IIRK) HEKLA LAVA 12 [hp_X] in 59 mL GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL 12 [hp_X] in 59 mL LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE 12 [hp_X] in 59 mL MANGANESE ACETATE TETRAHYDRATE (UNII: 9TO51D176N) (MANGANESE CATION (2+) - UNII:H6EP7W5457) MANGANESE ACETATE TETRAHYDRATE 12 [hp_X] in 59 mL MANGANESE CARBONATE (UNII: 9ZV57512ZM) (MANGANESE CATION (2+) - UNII:H6EP7W5457) MANGANESE CATION (2+) 12 [hp_X] in 59 mL MERCURY (UNII: FXS1BY2PGL) (MERCURY - UNII:FXS1BY2PGL) MERCURY 12 [hp_X] in 59 mL NITRIC ACID (UNII: 411VRN1TV4) (NITRIC ACID - UNII:411VRN1TV4) NITRIC ACID 12 [hp_X] in 59 mL PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN) PHOSPHORIC ACID 12 [hp_X] in 59 mL PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (PHYTOLACCA AMERICANA ROOT - UNII:11E6VI8VEG) PHYTOLACCA AMERICANA ROOT 12 [hp_X] in 59 mL LEAD IODIDE (UNII: OTL90F2GLT) (LEAD IODIDE - UNII:OTL90F2GLT) LEAD IODIDE 12 [hp_X] in 59 mL LEAD (UNII: 2P299V784P) (LEAD - UNII:2P299V784P) LEAD 12 [hp_X] in 59 mL SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 12 [hp_X] in 59 mL TARAXACUM OFFICINALE (UNII: 39981FM375) (TARAXACUM OFFICINALE - UNII:39981FM375) TARAXACUM OFFICINALE 12 [hp_X] in 59 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57955-2404-2 59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/10/2013 Labeler - King Bio Inc. (617901350) Registrant - King Bio Inc. (617901350) Establishment Name Address ID/FEI Business Operations King Bio Inc. 617901350 manufacture(57955-2404)
