Tropical

Manufacturer
Professional Complementary Health Formulas | Natural Pharmaceutical Manufacturing
Effective date
2019-08-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:15:40

Label at a glance#

ProductTropical 1022
Active ingredientSUS SCROFA ADRENAL GLAND, CORTICOTROPIN, HISTAMINE DIHYDROCHLORIDE, BEEF LIVER, ACACIA, CYNODON DACTYLON WHOLE, XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN, PLANTAGO LANCEOLATA LEAF, EUCALYPTUS GUM, POA PRATENSIS TOP, JUNIPERUS SCOPULORUM POLLEN, OLEA EUROPAEA FLOWER, AMARANTHUS HYBRIDUS LEAF, SYAGRUS ROMANZOFFIANA WHOLE, AMBROSIA ARTEMISIIFOLIA WHOLE, ATRIPLEX POLYCARPA WHOLE, WHITE MULBERRY
Label structure9 sections

Dosage and administration

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 1...

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

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

OTC - QUESTIONS SECTION

Professional Formulas

PO Box 2034 Lake Oswego, OR 97035

INDICATIONS

INDICATIONS & USAGE SECTION

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.*

OTC - PURPOSE SECTION

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

WARNINGS

WARNINGS SECTION

In case of overdose, get medical help or contact a poison control center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a healthcare professional before use.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

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

OTHER SAFETY 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

INACTIVE INGREDIENT SECTION

20% ethanol, purified water.

LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Est 1985

Professional Formulas

Complementary Health

Tropical

Homeopathic Remedy

2 FL. OZ. (59 mL)

Label imageLabel image

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7314d8f7-fa99-4dc2-9f68-de2ff142f4b7Product name220250121

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-1022-22026-01-09C16284748780-11030e365-645b-111a-e063-dadaa90a10e2ATH
63083-1022-22024-01-30C16284748780-11030e365-645b-111a-e063-dadaa90a10e2ATH

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63083-1022TROPICAL 1022 (TROPICAL) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]1Legacy NDC20220201_6a24e710-f0dc-4884-941c-bc46aee1e69f.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63083-102263083-1022-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
8f81cc1a-3129-4e85-9b4f-6b9f9e8e4f446a24e710-f0dc-4884-941c-bc46aee1e69f2026-01-08WarningsExact identifier
spl set id: 6a24e710-f0dc-4884-941c-bc46aee1e69f

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.