Label: INDUSTRIOX 6011- industriox liquid

  • 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 August 15, 2019

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  • ACTIVE INGREDIENTS

    Berberis vulgaris 3X
    Taraxacum officinale 3X
    Ammonium carbonicum 6X
    Camphora 6X
    Nux vomica 6X
    Sulphuricum acidum 6X, 12X
    Calcarea carbonica 12X
    Lachesis mutus 12X
    Plumbum metallicum 12X
    Acetonum 30X, 60X
    Acrylic resins 30X, 60X
    Benzinum 30X, 60X
    Carboneum chloratum 30X, 60X
    Chloroformum 30X, 60X
    Ethylmethyl ketone 30X, 60X
    Formalinum 30X, 60X
    Gasoline (MTBE) 30X, 60X
    Naphthalinum 30X, 60X
    Petroleum 30X, 60X
    Trichloroethylene 30X, 60X

  • QUESTIONS

    Professional Formulas

    PO Box 2034 Lake Oswego, OR 97035

  • INDICATIONS

    For the temporary relief of fatigue, lethargy, headaches, muscle or joint pain, mild bloating or gas, disturbed sleep, or lack of concentration due to sensitivity to or exposure to industrial chemicals, paint, petroleum, steel, and plastics.*

  • 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

    Industriox

    Homeopathic Remedy

    2 FL. OZ. (59 mL)

    Label image

  • INGREDIENTS AND APPEARANCE
    INDUSTRIOX  6011
    industriox liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63083-6011
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK3 [hp_X]  in 59 mL
    TARAXACUM OFFICINALE (UNII: 39981FM375) (TARAXACUM OFFICINALE - UNII:39981FM375) TARAXACUM OFFICINALE3 [hp_X]  in 59 mL
    AMMONIUM CATION (UNII: 54S68520I4) (AMMONIUM CATION - UNII:54S68520I4) AMMONIUM CATION6 [hp_X]  in 59 mL
    CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)6 [hp_X]  in 59 mL
    STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED6 [hp_X]  in 59 mL
    SULFURIC ACID (UNII: O40UQP6WCF) (SULFURIC ACID - UNII:O40UQP6WCF) SULFURIC ACID6 [hp_X]  in 59 mL
    OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE12 [hp_X]  in 59 mL
    LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) LACHESIS MUTA VENOM12 [hp_X]  in 59 mL
    LEAD (UNII: 2P299V784P) (LEAD - UNII:2P299V784P) LEAD12 [hp_X]  in 59 mL
    ACETONE (UNII: 1364PS73AF) (ACETONE - UNII:1364PS73AF) ACETONE30 [hp_X]  in 59 mL
    ACRYLIC ACID (UNII: J94PBK7X8S) (ACRYLIC ACID - UNII:J94PBK7X8S) ACRYLIC ACID30 [hp_X]  in 59 mL
    BENZENE (UNII: J64922108F) (BENZENE - UNII:J64922108F) BENZENE30 [hp_X]  in 59 mL
    CARBON TETRACHLORIDE (UNII: CL2T97X0V0) (CARBON TETRACHLORIDE - UNII:CL2T97X0V0) CARBON TETRACHLORIDE30 [hp_X]  in 59 mL
    CHLOROFORM (UNII: 7V31YC746X) (CHLOROFORM - UNII:7V31YC746X) CHLOROFORM30 [hp_X]  in 59 mL
    METHYL ETHYL KETONE (UNII: 6PT9KLV9IO) (METHYL ETHYL KETONE - UNII:6PT9KLV9IO) METHYL ETHYL KETONE30 [hp_X]  in 59 mL
    FORMALDEHYDE SOLUTION (UNII: T0H3L6C7I5) (FORMALDEHYDE SOLUTION - UNII:T0H3L6C7I5) FORMALDEHYDE SOLUTION30 [hp_X]  in 59 mL
    TERT-BUTYL METHYL ETHER (UNII: 29I4YB3S89) (TERT-BUTYL METHYL ETHER - UNII:29I4YB3S89) TERT-BUTYL METHYL ETHER30 [hp_X]  in 59 mL
    NAPHTHALENE (UNII: 2166IN72UN) (NAPHTHALENE - UNII:2166IN72UN) NAPHTHALENE30 [hp_X]  in 59 mL
    LIQUID PETROLEUM (UNII: 6ZAE7X688J) (LIQUID PETROLEUM - UNII:6ZAE7X688J) LIQUID PETROLEUM30 [hp_X]  in 59 mL
    TRICHLOROETHYLENE (UNII: 290YE8AR51) (TRICHLOROETHYLENE - UNII:290YE8AR51) TRICHLOROETHYLENE30 [hp_X]  in 59 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63083-6011-259 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product08/15/1985
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic08/15/1984
    Labeler - Professional Complementary Health Formulas (167339027)
    Registrant - Natural Pharmaceutical Manufacturing LLC (015624923)
    Establishment
    NameAddressID/FEIBusiness Operations
    Natural Pharmaceutical Manufacturing LLC015624923manufacture(63083-6011)
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