Label: ALLERGY NOSODE 4017- allergy nosode 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

If you are a consumer or patient please visit this version.

View All Sections
  • ACTIVE INGREDIENTS

    House dust mix 12X (15% by volume)
    Mold mix 12X (15% by volume)
    Grass mix 12X (10% by volume)
    Tree mix 12X (10% by volume)
    Weed mix 12X (10% by volume)
    Kali bichromicum 30X (5% by volume)
    Hepar sulphuris calcareum 12X (5% by volume)
    Histaminum 12X (5% by volume)
    Silicea 12X (5% by volume)
    Euphorbium officinalis 6X (5% by volume)
    Guaiacum 6X (5% by volume)
    Luffa operculata 6X (5% by volume)
    Sinapsis nigra 3X (5% by volume)

  • QUESTIONS

    Professional Formulas

    PO Box 2034 Lake Oswego, OR 97035

  • INDICATIONS

    For the temporary relief of runny nose, nasal congestion, headache, itchy or watery eyes, or mild facial or ear pain due to hay fever or other upper respiratory allergies.*

  • PURPOSE

    *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

  • WARNINGS

    If symptoms do not improve or are accompanied by a fever, consult a doctor. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use.

    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 to 15 drops once weekly or monthly. If mild symptoms are present, 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

    Allergy Nosode

    Homeopathic Remedy

    2 FL. OZ. (59 mL)

    Label image

  • INGREDIENTS AND APPEARANCE
    ALLERGY NOSODE  4017
    allergy nosode liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63083-4017
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOUSE DUST (UNII: EYO007VX98) (HOUSE DUST - UNII:EYO007VX98) HOUSE DUST12 [hp_X]  in 59 mL
    STACHYBOTRYS CHARTARUM (UNII: HJ4L70T1ZP) (STACHYBOTRYS CHARTARUM - UNII:HJ4L70T1ZP) STACHYBOTRYS CHARTARUM12 [hp_X]  in 59 mL
    MEDICAGO SATIVA WHOLE (UNII: DJO934BRBD) (MEDICAGO SATIVA WHOLE - UNII:DJO934BRBD) MEDICAGO SATIVA WHOLE12 [hp_X]  in 59 mL
    FRAXINUS LATIFOLIA WHOLE (UNII: 024W88F557) (FRAXINUS LATIFOLIA WHOLE - UNII:024W88F557) FRAXINUS LATIFOLIA WHOLE12 [hp_X]  in 59 mL
    TARAXACUM OFFICINALE (UNII: 39981FM375) (TARAXACUM OFFICINALE - UNII:39981FM375) TARAXACUM OFFICINALE12 [hp_X]  in 59 mL
    POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE30 [hp_X]  in 59 mL
    CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE12 [hp_X]  in 59 mL
    HISTAMINE (UNII: 820484N8I3) (HISTAMINE - UNII:820484N8I3) HISTAMINE12 [hp_X]  in 59 mL
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE12 [hp_X]  in 59 mL
    GUAIAC (UNII: 03C8A0DFJ8) (GUAIAC - UNII:03C8A0DFJ8) GUAIAC6 [hp_X]  in 59 mL
    LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU) (LUFFA OPERCULATA FRUIT - UNII:C4MO6809HU) LUFFA OPERCULATA FRUIT6 [hp_X]  in 59 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63083-4017-259 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(63083-4017)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!