Label: INDOOR AIR POLLUTION DETOX- acetaldehyde, ammonium causticum, carboneum oxygenisatum, chloroformum, formalinum, glycyrrhiza glabra, hydrastis canadensis, kali bichromicum, lycopodium clavatum, petroleum, plumbum metallicum, taraxacum officinale 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 May 28, 2014

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  • ACTIVE INGREDIENT

    Drug Facts​__________________________________________________________________________________________________________

    HPUS activeingredients: Acetaldehyde, Ammonium causticum, Carboneum oxygenisatum, Chloroformum, Formalinum, Glycyrrhiza glabra, Hydrastis canadensis, Kali bichromicum, Lycopodium clavatum, Petroleum, Plumbum metallicum, Taraxacum officinale. Equal volumes of each ingredient in 12X, 24X, LM1 potencies.

  • INDICATIONS & USAGE

    Uses temporarily relieves symptoms due to indoor air pollutants: breathing difficulties, eye, throat and lung irritation, fatigue, nausea, headaches.

  • INACTIVE INGREDIENT

    Inactive Ingredients: Bio-Energetically Enhanced™ pure water, citric acid and potassium sorbate.

  • WARNINGS

    Warnings

    • Stop use and ask your doctor if symptoms persist or worsen.
    • If pregnant or breast-feeding, ask a healthcare professional before use.
  • KEEP OUT OF REACH OF CHILDREN

    • Keep out of reach of children.
  • DOSAGE & ADMINISTRATION

    Directions

    • Initially, depress pump until primed.
    • Spray one dose directly into mouth.
    • Ages 12 and up: 3 sprays 3 times per day.
    • Ages 2-12: 2 sprays 3 times per day.
  • OTHER SAFETY INFORMATION

    Tamper resistant for your protection. Use only if safety seal is intact.

  • PURPOSE

    Uses temporarily relieves symptoms due to indoor air pollutants:

    • breathing difficulties
    • eye, throat and lung irritation
    • fatigue
    • nausea
    • headaches
  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    INDOOR AIR POLLUTION DETOX 
    acetaldehyde, ammonium causticum, carboneum oxygenisatum, chloroformum, formalinum, glycyrrhiza glabra, hydrastis canadensis, kali bichromicum, lycopodium clavatum, petroleum, plumbum metallicum, taraxacum officinale liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57955-6001
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETALDEHYDE (UNII: GO1N1ZPR3B) (ACETALDEHYDE - UNII:GO1N1ZPR3B) ACETALDEHYDE12 [hp_X]  in 59 mL
    AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X) AMMONIA12 [hp_X]  in 59 mL
    CARBON MONOXIDE (UNII: 7U1EE4V452) (CARBON MONOXIDE - UNII:7U1EE4V452) CARBON MONOXIDE12 [hp_X]  in 59 mL
    CHLOROFORM (UNII: 7V31YC746X) (CHLOROFORM - UNII:7V31YC746X) CHLOROFORM12 [hp_X]  in 59 mL
    FORMALDEHYDE (UNII: 1HG84L3525) (FORMALDEHYDE - UNII:1HG84L3525) FORMALDEHYDE12 [hp_X]  in 59 mL
    GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) (GLYCYRRHIZA GLABRA - UNII:2788Z9758H) GLYCYRRHIZA GLABRA12 [hp_X]  in 59 mL
    GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL12 [hp_X]  in 59 mL
    POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE12 [hp_X]  in 59 mL
    LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE12 [hp_X]  in 59 mL
    KEROSENE (UNII: 1C89KKC04E) (KEROSENE - UNII:1C89KKC04E) KEROSENE12 [hp_X]  in 59 mL
    LEAD (UNII: 2P299V784P) (LEAD - UNII:2P299V784P) LEAD12 [hp_X]  in 59 mL
    TARAXACUM OFFICINALE (UNII: 39981FM375) (TARAXACUM OFFICINALE - UNII:39981FM375) TARAXACUM OFFICINALE12 [hp_X]  in 59 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57955-6001-259 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic05/28/2014
    Labeler - King Bio Inc. (617901350)
    Registrant - King Bio Inc. (617901350)
    Establishment
    NameAddressID/FEIBusiness Operations
    King Bio Inc.617901350manufacture(57955-6001)
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