FDA.reportPublic FDA data

Menthol

Manufacturer
Target Corporation
Effective date
2024-12-11
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 20:46:57

Label at a glance#

ProductMenthol
Active ingredientMENTHOL
Label structure8 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, 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 irritation 

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes

Stop and consult 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

In case of accidental ingestion, 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, 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

benzathonium Chloride, eucalyptus oil, peppermint oil, sodium bicarbonate, tricalcium phosphate, zea mays (corn) starch

Questions?

OTC - QUESTIONS SECTION

Call 1-800-910-6874

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

maximum strength

medicated

foot powder

menthol 1 %

external analgesic

talc- free

triple action formula absorbs moisture,

relieve itching and helps control foot odor

NET WT 10 OZ (283 g)

medicated powdermedicated powder

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11673-511-102023-01-31C16284748780-1f386c649-a71e-0266-e053-dadaa90a7c1aMedicated Foot Powder -Talc Free
11673-511-102023-01-30C16284748780-1f386c649-a71e-0266-e053-dadaa90a7c1aMedicated Foot Powder -Talc Free

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-511MENTHOL (MAXIMUM STRENGTH MEDICATED FOOT POWDER TALC FREE) POWDER [TARGET CORPORATION]6Legacy NDC20241213_cee20e8e-3a44-437b-83ef-0f5303fece2a.zip

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
11673-51111673-511-10

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
ZEA MAYS SUBSP. MAYS WHOLE1G5HNE09V8IACT
TRICALCIUM PHOSPHATEK4C08XP666IACT
SODIUM BICARBONATE8MDF5V39QOIACT
BENZETHONIUM CHLORIDEPH41D05744IACT
EUCALYPTUS OIL2R04ONI662IACT
PEPPERMINT OILAV092KU4JHIACT
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
37c8daa2-6b8d-05ac-e063-6294a90a8154cee20e8e-3a44-437b-83ef-0f5303fece2a2025-06-17WarningsExact identifier
spl set id: cee20e8e-3a44-437b-83ef-0f5303fece2a

Reported adverse events (FAERS/openFDA)#

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