FDA.reportPublic FDA data

Menthol

Manufacturer
VALU MERCHANDISERS, CO
Effective date
2019-11-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:56:14

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 on the foot

​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

benzethonium chloride, eucalytus oil, gum acacia, peppermint oil, sodium bicarbonate, talc

​Questions?

OTC - QUESTIONS SECTION

Call 1-866-964-0939

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Best Choice

Medicated

Foot Powder

Menthol 1.0% External Analgesic

Triple Relief Formula

  • Absorbs Moisture
  • Relieves Itching
  • Controls Foot Odor

NET WT 10 OZ (283 g)

Best Choice_Medicated Foot Powder_50-113BC_51-113BC.jpgBest Choice_Medicated Foot Powder_50-113BC_51-113BC.jpg

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
63941-55263941-552-10

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
BENZETHONIUM CHLORIDEPH41D05744IACT
EUCALYPTUS OIL2R04ONI662IACT
ACACIA5C5403N26OIACT
PEPPERMINT OILAV092KU4JHIACT
SODIUM BICARBONATE8MDF5V39QOIACT
TALC7SEV7J4R1UIACT
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
f2277e27-868d-57ef-e053-2a95a90abf2801512e67-c433-4808-9d50-4950e1e943792023-01-13WarningsExact identifier
spl set id: 01512e67-c433-4808-9d50-4950e1e94379

Reported adverse events (FAERS/openFDA)#

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