FDA.reportPublic FDA data

Maximum Strength Medicated Foot Powder

Manufacturer
Davion, Inc
Effective date
2025-12-29
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:29:18

Label at a glance#

ProductMaximum Strength Medicated Foot Powder
Active ingredientMENTHOL
Label structure7 sections

Indications and uses

Temporary relief of pain and itch associated with: minor cuts sunburn insect bites scrapes minor burns minor skin irritations

Dosage and administration

Remove seal beneath cap before first use. Do not use if seal is broken adults and children 2 years and older - apply freely upto 3 or 4 times daily children under 2 years - ask a doctor For best results, dry skin throughly before applying

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 1.0%

Purpose

OTC - PURPOSE SECTION

External Analgesic

Uses

INDICATIONS & USAGE SECTION

Temporary relief of pain and itch associated with:

  • minor cuts
  • sunburn
  • insect bites
  • scrapes
  • minor burns
  • minor skin irritations

Warning

WARNINGS SECTION

  • For external use only
  • Avoid contact with eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms persist for more than 7 days or clear up and occur again within 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

Remove seal beneath cap before first use. Do not use if seal is broken

  • adults and children 2 years and older - apply freely upto 3 or 4 times daily
  • children under 2 years - ask a doctor

For best results, dry skin throughly before applying

Inactive ingredients

INACTIVE INGREDIENT SECTION

Zea Mays (Corn) Starch, Tricalcium Phosphate,  Sodium Bicarbonate, Benzethonium Chloride, Eucalyptus Oil, Peppermint Oil

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 42669-283-01

CVS HEALTH Compared to the active ingredient in Maximum Strength Gold bond Medicated Foot Powder*

MAXIMUM STRENGTH Medicated Foot Powder WITH CORNSTARCG

  • Triple Relief: controls odor, absorbs moisture & relieves itc
  • Soothing formula
  • Clinically tested
  • Talc free

NET WT 10 OZ (283 g)

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
259579menthol 1 % Topical PowderPSN5
259579menthol 0.01 MG/MG Topical PowderSCD5
259579menthol 1 % Topical PowderSY5

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
42669-283-012024-02-28C16284748780-11030e365-5430-111a-e063-dadaa90a10e2MAXIMUM STRENGTH Medicated Foot Powder with Corn Starch
42669-283-012024-01-30C16284748780-11030e365-5430-111a-e063-dadaa90a10e2MAXIMUM STRENGTH Medicated Foot Powder with Corn Starch

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42669-283-01Maximum Strength Medicated Foot Powder283 g in 1 BOTTLEPOWDER2835

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
42669-28342669-283-01

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
STARCH, CORNO8232NY3SJIACT
TRICALCIUM PHOSPHATEK4C08XP666IACT
SODIUM BICARBONATE8MDF5V39QOIACT
EUCALYPTUS OIL2R04ONI662IACT
BENZETHONIUM CHLORIDEPH41D05744IACT
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
Maximum Strength Medicated Foot PowderMENTHOLDavion, Inc7b442d99-ac19-4f65-828d-954c5350ef5a2025-12-29WarningsExact identifier
ndc (package): 42669-283-01
ndc (product): 42669-283
ndc11 (package): 42669028301
spl id: 9df9d907-df74-40b5-8462-c90a3e2e288d
spl set id: 7b442d99-ac19-4f65-828d-954c5350ef5a

Reported adverse events (FAERS/openFDA)#

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