FDA.reportPublic FDA data

TriDerma Tea Tree Foot Cream

Manufacturer
Genuine Virgin Aloe Corporation
Effective date
2026-01-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:36:06

Label at a glance#

ProductTriDerma Tea Tree Foot Cream
Active ingredientMENTHOL
Label structure10 sections

Indications and uses

for the temporary relief of pain and burning.  Can help distract from pain.  May provide a cooling sensation

Dosage and administration

On clean skin, apply to feet, heels and legs twice a day or as often as needed.

Label contents#

Full prescribing information#

WARNINGS

WARNINGS SECTION

For external use only

PURPOSE

OTC - PURPOSE SECTION

Topical Analgesic

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

On clean skin, apply to feet, heels and legs twice a day or as often as needed.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Allantoin, Aloe Barbadensis Leaf Juice*, Butyrospermum Parkii (Shea) Butter, Cera Alba (Beeswax), Cetearyl Alcohol, Cetyl Alcohol, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Colloidal Oatmeal, Dimethicone, Ethylhexylglycerin, Isopropyl Palmitate, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Panthenol (Pro-Vitamin B5), Phenoxyethanol, Polysorbate 60, Salicylic Acid, Sodium Hyaluronate, Sodium Hydroxide, Sodium PCA, Sodium Phytate, Tocopheryl Acetate (Vitamin E), Urea, Water, Zinc PCA.

*Certified Organic Ingredient - Mayacert Certifier

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Menthol 1.0%

USES

INDICATIONS & USAGE SECTION

for the temporary relief of pain and burning.  Can help distract from pain.  May provide a cooling sensation

WHEN USING THIS PRODUCT:

OTC - WHEN USING SECTION

avoid contact with eyes

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed get medical help and contact a Poison Control Center right away.

STOP USE AND ASK A DOCTOR IF:

OTC - STOP USE SECTION

condition worsens or does not improve within 7 days.

PACKAGING

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

tt foottt foot

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2475473menthol 1 % Topical CreamPSN1
2475473menthol 10 MG/ML Topical CreamSCD1
2475473menthol 1 % Topical CreamSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130818926014502GTIN-13: 0818926014502
EAN-13: 0818926014502
GTIN-12: 818926014502
UPC-A: 818926014502
GTIN storage (14 digits): 00818926014502		tt foot.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10738-011-91TriDerma Tea Tree Foot Cream270 g in 1 JARCREAM2701

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10738-01110738-011-91

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIMETHICONE 100RO266O364UIACT
BEESWAX2ZA36H0S2VIACT
ALOE VERA LEAF JUICERUE8E6T4NBIACT
SHEA BUTTERK49155WL9YIACT
ALLANTOIN344S277G0ZIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
CETEARYL ALCOHOL2DMT128M1SIACT
OATMEAL8PI54V663YIACT
CETYL ALCOHOL936JST6JCNIACT
SODIUM PCA469OTG57A2IACT
BERGAMOT OIL39W1PKE3JIIACT
TEA TREE OILVIF565UC2GIACT
SODIUM HYALURONATEYSE9PPT4THIACT
MENTHOLL7T10EIP3AACTIB

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
TriDerma Tea Tree Foot CreamTTM FOOTGenuine Virgin Aloe Corporation49b51d5f-14d1-a5c6-e063-6294a90abdab2026-01-31WarningsExact identifier
ndc (package): 10738-011-91
ndc (product): 10738-011
ndc11 (package): 10738001191
spl id: 49b51d77-315a-90ef-e063-6394a90a1199
spl set id: 49b51d5f-14d1-a5c6-e063-6294a90abdab

Reported adverse events (FAERS/openFDA)#

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