FDA.reportPublic FDA data

Medicated Foot Powder -Talc Free

Manufacturer
Target Corporation
Effective date
2026-10-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-10-06 02:04:38

Label at a glance#

ProductMenthol
Active ingredientMENTHOL
Label structure9 sections

Dosage and administration

adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily children under 2 years of age: do not use, consult a doctor wash and dry feet thoroughly sprinkle powder liberally on feet, between toes and on bottoms of feet

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 1.0%

Purpose

OTC - PURPOSE SECTION

External analgesic

Use

INDICATIONS & USAGE SECTION

for the temporary relief of pain and itching associated with minor skin irritations

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

  • conditions worsens
  • symptoms persists for more than 7 days or clear up and occur again within a few days

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
  • children under 2 years of age: do not use, consult a doctor
  • wash and dry feet thoroughly
  • sprinkle powder liberally on feet, between toes and on bottoms of feet

Inactive ingredients

INACTIVE INGREDIENT SECTION

zea mays (corn) starch, sodium bicarbonate, tricalcium phosphate, benzethonium chloride, eucalyptus globulus leaf oil, mentha piperita (peppermint) oil

Questions?

OTC - QUESTIONS SECTION

Call 1-866-964-0939

RECENT MAJOR CHANGES SECTION

..

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Compare to active ingredient in Gold Bond

Medicated Foot Powder

Maximum Strength

Medicated

Foot Powder

Menthol 1 %- External Analgesic

  • Triple- action formula absorbs

moisture, relieves itching and

helps control foot odor

  • Talc free

up&up

NET WT. 10 OZ. (283 g)

cartoncarton

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130034197011242GTIN-13: 0034197011242
EAN-13: 0034197011242
GTIN-12: 034197011242
UPC-A: 034197011242
GTIN storage (14 digits): 00034197011242		Target_upup_Medicated Foot Powder_50-113TG-02_51-113TG-02.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82442-21182442-211-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AACTIB
TRICALCIUM PHOSPHATEK4C08XP666IACT
SODIUM BICARBONATE8MDF5V39QOIACT
BENZETHONIUM CHLORIDEPH41D05744IACT
EUCALYPTUS GLOBULUS LEAF OIL2R04ONI662IACT
MENTHA PIPERITA (PEPPERMINT) OILAV092KU4JHIACT
ZEA MAYS (CORN) STARCHO8232NY3SJIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-11-06full-release2026-06-01 01:42:32
12025-05-27full-release2026-06-01 01:01:59

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
42f3fbdb-8110-35e8-e063-6394a90a5f53365fca57-2107-727d-e063-6394a90a070d2025-11-06WarningsExact identifier
spl set id: 365fca57-2107-727d-e063-6394a90a070d

Reported adverse events (FAERS/openFDA)#

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