FDA.reportPublic FDA data

WHP Fungus

Manufacturer
Washington Homeopathic Products
Effective date
2025-01-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:31:36

Label at a glance#

ProductWHP Fungus
Active ingredientTHUJA OCCIDENTALIS LEAFY TWIG, KEROSENE, SULFUR
Label structure8 sections

Indications and uses

Temporarily relieves itching eruptions of the skin, as in ringworm or athlete's foot.

Dosage and administration

Directions: Adults and children 12 years and older: 2 pills dissolved under tongue every 4 hours, or as directed by a licensed practitioner. Children 4 years to under 12 years: 1 pill dissolved under tongue every 4 hours, or as directed by a licensed practitioner. Children under 4 years: Consult a licensed practitioner.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

PETROLEUM 6C

SULPHUR 6C

THUJA OCC 6C

USES

OTC - PURPOSE SECTION

Temporarily relieves itching eruptions of the skin, as in ringworm or athlete's foot.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

As with all medications, keep out of reach of children.

INDICATIONS

INDICATIONS & USAGE SECTION

PETROLEUM Nausea

SULPHUR Skin problems

THUJA OCC Warts

STOP USE AND ASK DOCTOR

WARNINGS SECTION

If symptoms persist or recur, discontinue use. If pregnant or nursing, consult a licensed practitioner before using this product.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Directions: Adults and children 12 years and older: 2 pills dissolved under tongue every 4 hours, or as directed by a licensed practitioner. Children 4 years to under 12 years: 1 pill dissolved under tongue every 4 hours, or as directed by a licensed practitioner. Children under 4 years: Consult a licensed practitioner.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Sucrose/Lactose

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WHP Fungus labelWHP Fungus labelWHP Fungus boxWHP Fungus box

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71919-806-14WHP Fungus1 in 1 BOXPELLET12
71919-806-14WHP Fungus1 in 1 BOTTLE, PLASTICPELLET12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71919-806WHP FUNGUS (KEROSENE - SULFUR - THUJA OCCIDENTALIS LEAFY) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]2Current NDC, 2 package rows20250130_06d446a8-2fc0-fea1-e063-6394a90a835e.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71919-80671919-806-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUCROSEC151H8M554IACT
LACTOSEJ2B2A4N98GIACT
THUJA OCCIDENTALIS LEAFY TWIG1NT28V9397ACTIB
KEROSENE1C89KKC04EACTIB
SULFUR70FD1KFU70ACTIB

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
WHP FungusKEROSENE - SULFUR - THUJA OCCIDENTALIS LEAFYWashington Homeopathic Products06d446a8-2fc0-fea1-e063-6394a90a835e2025-01-28WarningsExact identifier
ndc (package): 71919-806-14
ndc (product): 71919-806
ndc11 (package): 71919080614
spl id: 2cc8665c-5c37-a931-e063-6294a90ade88
spl set id: 06d446a8-2fc0-fea1-e063-6394a90a835e

Reported adverse events (FAERS/openFDA)#

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