Label: TROPICAL 1022- tropical 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

    Adrenal 6X
    ACTH 6X, 30X
    Histaminum hydrochloricum 12X
    Liver 6X, 12X
    and all the following at 6X, 12X, 60X, 100X:
    Acacia
    Bermuda grass
    Cocklebur
    English plantain
    Eucalyptus
    Kentucky bluegrass
    Mountain cedar
    Olive pollen
    Pigweed mix
    Queen palm
    Ragweed
    Saltbush
    White mulberry

  • QUESTIONS

    Professional Formulas

    PO Box 2034 Lake Oswego, OR 97035

  • INDICATIONS

    For the temporary relief of runny nose, sneezing, itching of the nose or throat, and itchy, watery eyes due to sensitivity to common allergens in the tropics and Hawaii.*

  • 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 to 15 drops up to 3 times per day. For desensitization, begin with 1 to 5 drops daily, increasing to the standard dose gradually to avoid symptom expression; after 1 to 3 months at the standard dose, decrease gradually to a maintenance dose of 10 to 15 drops weekly. 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

    Tropical

    Homeopathic Remedy

    2 FL. OZ. (59 mL)

    Label image

  • INGREDIENTS AND APPEARANCE
    TROPICAL  1022
    tropical liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63083-1022
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (SUS SCROFA ADRENAL GLAND - UNII:398IYQ16YV) SUS SCROFA ADRENAL GLAND6 [hp_X]  in 59 mL
    CORTICOTROPIN (UNII: K0U68Q2TXA) (CORTICOTROPIN - UNII:K0U68Q2TXA) CORTICOTROPIN6 [hp_X]  in 59 mL
    HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE12 [hp_X]  in 59 mL
    BEEF LIVER (UNII: W8N8R55022) (BEEF LIVER - UNII:W8N8R55022) BEEF LIVER6 [hp_X]  in 59 mL
    ACACIA (UNII: 5C5403N26O) (ACACIA - UNII:5C5403N26O) ACACIA6 [hp_X]  in 59 mL
    CYNODON DACTYLON WHOLE (UNII: 2Q8MR21NHK) (CYNODON DACTYLON WHOLE - UNII:2Q8MR21NHK) CYNODON DACTYLON WHOLE6 [hp_X]  in 59 mL
    XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN (UNII: 0ZK6G3W3BI) (XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN - UNII:0ZK6G3W3BI) XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN6 [hp_X]  in 59 mL
    PLANTAGO LANCEOLATA LEAF (UNII: 2YWL9J7EE8) (PLANTAGO LANCEOLATA LEAF - UNII:2YWL9J7EE8) PLANTAGO LANCEOLATA LEAF6 [hp_X]  in 59 mL
    EUCALYPTUS GUM (UNII: 72T9EZC2VX) (EUCALYPTUS GUM - UNII:72T9EZC2VX) EUCALYPTUS GUM6 [hp_X]  in 59 mL
    POA PRATENSIS TOP (UNII: 7EA48700V9) (POA PRATENSIS TOP - UNII:7EA48700V9) POA PRATENSIS TOP6 [hp_X]  in 59 mL
    JUNIPERUS SCOPULORUM POLLEN (UNII: 0G82TT8ZFY) (JUNIPERUS SCOPULORUM POLLEN - UNII:0G82TT8ZFY) JUNIPERUS SCOPULORUM POLLEN6 [hp_X]  in 59 mL
    OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ) (OLEA EUROPAEA FLOWER - UNII:498M34P1VZ) OLEA EUROPAEA FLOWER6 [hp_X]  in 59 mL
    AMARANTHUS HYBRIDUS LEAF (UNII: 07L86FJ69J) (AMARANTHUS HYBRIDUS LEAF - UNII:07L86FJ69J) AMARANTHUS HYBRIDUS LEAF6 [hp_X]  in 59 mL
    SYAGRUS ROMANZOFFIANA WHOLE (UNII: 3I21564JAW) (SYAGRUS ROMANZOFFIANA WHOLE - UNII:3I21564JAW) SYAGRUS ROMANZOFFIANA WHOLE6 [hp_X]  in 59 mL
    AMBROSIA ARTEMISIIFOLIA WHOLE (UNII: 9W34L2CQ9A) (AMBROSIA ARTEMISIIFOLIA WHOLE - UNII:9W34L2CQ9A) AMBROSIA ARTEMISIIFOLIA WHOLE6 [hp_X]  in 59 mL
    ATRIPLEX POLYCARPA WHOLE (UNII: 12IGX5TK1H) (ATRIPLEX POLYCARPA WHOLE - UNII:12IGX5TK1H) ATRIPLEX POLYCARPA WHOLE6 [hp_X]  in 59 mL
    WHITE MULBERRY (UNII: MN25R0HH5A) (WHITE MULBERRY - UNII:MN25R0HH5A) WHITE MULBERRY6 [hp_X]  in 59 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63083-1022-259 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 (015624923)
    Establishment
    NameAddressID/FEIBusiness Operations
    Natural Pharmaceutical Manufacturing015624923manufacture(63083-1022)
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