FDA.reportPublic FDA data

Maximum Strength Medicated Foot Powder

Manufacturer
Walmart Stores Inc
Effective date
2025-12-27
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:28:55

Label at a glance#

ProductMaximum Strength Medicated Foot Powder
Active ingredientMENTHOL
Label structure7 sections

Dosage and administration

adults and children 2 years of age and over: apply freely up to 3 or 4 times daily children under 2 years: consult a physician For best results, dry skin thoroughly before use.

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 cuts

-scrapes

-sunburn

-insect bites

-prickly heat

-rashes

-minor burns

-minor skin irritation

-dries the oozing of poison ivy, oak and sumac.

​Warnings

WARNINGS SECTION

​For external use only.

​When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes. Not for genital area

Stop and consult a doctor if

OTC - ASK DOCTOR SECTION

  • conditions worsens
  • redness, irritation, swelling or pain persist or increases
  • symptoms do not get better within 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 (1-800-222-1222) right away.

​Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 2 years of age and over: apply freely up to 3 or 4 times daily
  • children under 2 years: consult a physician
  • For best results, dry skin thoroughly before use.

​Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Maximum Strength Medicated Foot Powder

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
259579menthol 1 % Topical PowderPSN4
259579menthol 0.01 MG/MG Topical PowderSCD4
259579menthol 1 % Topical PowderSY4

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49035-795-01Maximum Strength Medicated Foot Powder283 g in 1 BOTTLE, PLASTICPOWDER2834

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49035-79549035-795-01

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
BENZETHONIUM CHLORIDEPH41D05744IACT
EUCALYPTUS OIL2R04ONI662IACT
TRICALCIUM PHOSPHATEK4C08XP666IACT
PEPPERMINT OILAV092KU4JHIACT
SODIUM BICARBONATE8MDF5V39QOIACT
ZEA MAYS WHOLE1G5HNE09V8IACT
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
Maximum Strength Medicated Foot PowderMEDICATED FOOT POWDERWalmart Stores Incb0794d48-eb8b-55c9-e053-2995a90a5b382025-12-27WarningsExact identifier
ndc (package): 49035-795-01
ndc (product): 49035-795
ndc11 (package): 49035079501
spl id: 46f6ba22-d323-2610-e063-6394a90a486a
spl set id: b0794d48-eb8b-55c9-e053-2995a90a5b38

Reported adverse events (FAERS/openFDA)#

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