FDA.reportPublic FDA data

Menthol

Manufacturer
VALU MERCHANDISERS, CO
Effective date
2025-11-24
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 01:17:52

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 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: 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

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

​Questions?

OTC - QUESTIONS SECTION

Call 1-866-964-0939

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Best Choice

MAXIMUM STRENGTH

Medicated Foot Powder

MENTHOL 1.0% / EXTERNAL ANALGESIC

TALC-FREE

  • Absorbs Moisture
  • Relieves Itching
  • Helps Control Foot Odor

NET WT 10 oz (283g)

best choicebest choice

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
259579menthol 1 % Topical PowderPSN8
259579menthol 0.01 MG/MG Topical PowderSCD8
259579menthol 1 % Topical PowderSY8

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63941-558-102024-02-20C16284748780-1f386c649-c1b1-0266-e053-dadaa90a7c1aMedicated Foot Powder -Talc Free
63941-558-102024-02-20C16284748780-1f386c649-c1b1-0266-e053-dadaa90a7c1aMedicated Foot Powder -Talc Free
63941-558-102023-01-30C16284748780-1f386c649-c1b1-0266-e053-dadaa90a7c1aMedicated Foot Powder -Talc Free
63941-558-102023-01-30C16284748780-1f386c649-c1b1-0266-e053-dadaa90a7c1aMedicated Foot Powder -Talc Free

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63941-558-10Menthol283 g in 1 BOTTLE, PLASTICPOWDER2838

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
63941-55863941-558-10

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
STARCH, CORNO8232NY3SJIACT
PEPPERMINT OILAV092KU4JHIACT
SODIUM BICARBONATE8MDF5V39QOIACT
TRICALCIUM PHOSPHATEK4C08XP666IACT
MENTHOLL7T10EIP3AACTIB
EUCALYPTUS OIL2R04ONI662IACT
BENZETHONIUM CHLORIDEPH41D05744IACT

Source Document#

Source XML · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
62024-11-07full-release2026-06-01 00:35:41

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
MentholMAXIMUM STRENGTH MEDICATED FOOT POWDERVALU MERCHANDISERS, CO89a5c4bb-442f-d3f0-e053-2a95a90a51bd2025-11-24WarningsExact identifier
ndc (package): 63941-558-10
ndc (product): 63941-558
ndc11 (package): 63941055810
spl id: 445c7a07-4f2a-f717-e063-6394a90ac462
spl set id: 89a5c4bb-442f-d3f0-e053-2a95a90a51bd

Reported adverse events (FAERS/openFDA)#

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