Menthol

Manufacturer
FSA Store Inc.
Effective date
2023-05-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:31:52

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 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

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

benzathonium 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

Caring Mill

maximum strength

medicated

foot powder

external analgesic/menthol 1 %

talc- free

triple action formula

  • absorbs moisture
  • relieve itching
  • helps control foot odor

NET WT 10 OZ (283 g)

image 1image 1

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
81522-07581522-075-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
29ba8554-c5f1-4a05-e063-6394a90a520efabc23eb-7750-1b5a-e053-6294a90aed032024-12-20WarningsExact identifier
spl set id: fabc23eb-7750-1b5a-e053-6294a90aed03

Reported adverse events (FAERS/openFDA)#

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