Label: INDUSTRIOX (berberis vulgaris, taraxacum officinale, ammonium carbonicum, camphora, spinacia, sulphuricum acidum, nux vomica, acetone, benzinum, butyl methacrylate, calcarea carbonica, lachesis mutus, methyl ethyl ketone, naphthalinum, plumbum metallicum, trichloroethylene, forlmalinum, mtbe- tert-butyl methyl ether, petroleum, carboneum chloratum spray
- NDC Code(s): 83027-0048-1
- Packager: Nutritional Specialties, Inc.
- Category: HUMAN OTC DRUG LABEL
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 September 25, 2023
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ACTIVE INGREDIENTS:
Berberis Vulgaris 3X, Taraxacum Officinale 3X, Ammonium Carbonicum 6X, Camphora 6X, Spinacia 6X, Sulphuricum Acidum 6X, 12X, Nux Vomica 8X, Acetone 12X, Benzinum 12X, Butyl Methacrylate 12X, Calcarea Carbonica 12X, Lachesis Mutus 12X, Methyl Ethyl Ketone 12X, Naphthalinum 12X, Plumbum Metallicum 12X, Trichloroethylene 12X, Forlmalinum 12X, 30X, MTBE 16X, 20X, 30X, 60X, Petroleum 16X, 20X, 30X, 60X, Carboneum Chloratum 20X.
- PURPOSE:
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WARNINGS:
Professional Use Only
If pregnant or breast-feeding, ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away.
If condition worsens, seek medical attention.
KEEP OUT OF REACH OF CHILDREN
Do not use if tamper evident seal is broken or missing.
Store in a cool place after opening
- KEEP OUT OF REACH OF CHILDREN:
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DIRECTIONS:
Adults: 2 to 3 sprays orally, three times daily. Children under twelve one half adult dosage. For highly sensitive individuals: best tolerated administration is through imbrication (RUBBING IN) on skin at pulse points or abdomen. Do not take within 15 minutes of consuming food, beverage or brushing teeth. Consult a physician for use in children under 12 years of age.
- INDICATIONS:
- INACTIVE INGREDIENTS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY:
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INGREDIENTS AND APPEARANCE
INDUSTRIOX
berberis vulgaris, taraxacum officinale, ammonium carbonicum, camphora, spinacia, sulphuricum acidum, nux vomica, acetone, benzinum, butyl methacrylate, calcarea carbonica, lachesis mutus, methyl ethyl ketone, naphthalinum, plumbum metallicum, trichloroethylene, forlmalinum, mtbe (tert-butyl methyl ether), petroleum, carboneum chloratum sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83027-0048 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK 3 [hp_X] in 1 mL TARAXACUM OFFICINALE (UNII: 39981FM375) (TARAXACUM OFFICINALE - UNII:39981FM375) TARAXACUM OFFICINALE 3 [hp_X] in 1 mL AMMONIUM CARBONATE (UNII: NJ5VT0FKLJ) (AMMONIUM CATION - UNII:54S68520I4) AMMONIUM CARBONATE 6 [hp_X] in 1 mL CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL) 6 [hp_X] in 1 mL SPINACIA OLERACEA ROOT (UNII: A19RZC6BEH) (SPINACIA OLERACEA ROOT - UNII:A19RZC6BEH) SPINACIA OLERACEA ROOT 6 [hp_X] in 1 mL SULFURIC ACID (UNII: O40UQP6WCF) (SULFURIC ACID - UNII:O40UQP6WCF) SULFURIC ACID 6 [hp_X] in 1 mL STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 8 [hp_X] in 1 mL ACETONE (UNII: 1364PS73AF) (ACETONE - UNII:1364PS73AF) ACETONE 12 [hp_X] in 1 mL BENZENE (UNII: J64922108F) (BENZENE - UNII:J64922108F) BENZENE 12 [hp_X] in 1 mL N-BUTYL METHACRYLATE (UNII: R5QX287XXU) (N-BUTYL METHACRYLATE - UNII:R5QX287XXU) N-BUTYL METHACRYLATE 12 [hp_X] in 1 mL OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X] in 1 mL LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) LACHESIS MUTA VENOM 12 [hp_X] in 1 mL METHYL ETHYL KETONE (UNII: 6PT9KLV9IO) (METHYL ETHYL KETONE - UNII:6PT9KLV9IO) METHYL ETHYL KETONE 12 [hp_X] in 1 mL NAPHTHALENE (UNII: 2166IN72UN) (NAPHTHALENE - UNII:2166IN72UN) NAPHTHALENE 12 [hp_X] in 1 mL LEAD (UNII: 2P299V784P) (LEAD - UNII:2P299V784P) LEAD 12 [hp_X] in 1 mL TRICHLOROETHYLENE (UNII: 290YE8AR51) (TRICHLOROETHYLENE - UNII:290YE8AR51) TRICHLOROETHYLENE 12 [hp_X] in 1 mL FORMALDEHYDE SOLUTION (UNII: T0H3L6C7I5) (FORMALDEHYDE SOLUTION - UNII:T0H3L6C7I5) FORMALDEHYDE SOLUTION 12 [hp_X] in 1 mL TERT-BUTYL METHYL ETHER (UNII: 29I4YB3S89) (TERT-BUTYL METHYL ETHER - UNII:29I4YB3S89) TERT-BUTYL METHYL ETHER 16 [hp_X] in 1 mL KEROSENE (UNII: 1C89KKC04E) (KEROSENE - UNII:1C89KKC04E) KEROSENE 16 [hp_X] in 1 mL CARBON TETRACHLORIDE (UNII: CL2T97X0V0) (CARBON TETRACHLORIDE - UNII:CL2T97X0V0) CARBON TETRACHLORIDE 20 [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:83027-0048-1 60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 09/25/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/25/2023 Labeler - Nutritional Specialties, Inc. (032744609)