FDA.reportPublic FDA data

Maximum Strength Medicated Foot Powder

Manufacturer
CVS | Davion, Inc
Effective date
2018-01-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:03:10

Label at a glance#

ProductMaximum Strength Medicated Foot Powder
Active ingredientMENTHOL
Label structure7 sections

Indications and uses

Temporary relief of pain and itch associate 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 associate 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 69842-283-01

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

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
69842-28369842-283-01

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

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
0e24855a-6c52-5087-e063-6394a90ae1c722e9b151-3020-4202-af27-d73fdaf9377c2024-01-04WarningsExact identifier
spl set id: 22e9b151-3020-4202-af27-d73fdaf9377c

Reported adverse events (FAERS/openFDA)#

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