FDA.reportPublic FDA data

Meijer Medicated Foot Powder

Manufacturer
Meijer Distribution | Jell Pharmaceuticals
Effective date
2024-07-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:16:09

Label at a glance#

ProductMeijer Medicated Foot Powder
Active ingredientMENTHOL
Label structure8 sections

Indications and uses

for the temporary relief of the pain and itch 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.

Dosage and administration

Directions ■ 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%

Purpose

OTC - PURPOSE SECTION

External analgesic

Uses

INDICATIONS & USAGE SECTION


for the temporary relief of the pain and itch 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 use and consult a doctor if

OTC - STOP USE SECTION

■ Condition worsens ■ Redness, irritation, swelling or pain persists 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

Keep out of reach of children.
In case of accidental ingestion, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions
■ 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

Inactive ingredients
benzethonium chloride, eucalyptus oil, peppermint oil, sodium bicarbonate, tricalcium phospate, zea mays (corn) starch

Questions or comments

OTC - QUESTIONS SECTION

Call toll-free 1-866-326-1313

Meijer Medicated Foot Powder, 10 oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
259579menthol 1 % Topical PowderPSN2
259579menthol 0.01 MG/MG Topical PowderSCD2
259579menthol 1 % Topical PowderSY2

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
79481-0043-1Meijer Medicated Foot Powder283 g in 1 BOTTLEPOWDER2832

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79481-0043MEIJER MEDICATED FOOT POWDER (MENTHOL) POWDER [MEIJER DISTRIBUTION]2Current NDC, 1 package rows20240730_07ec6c20-73c4-e5e4-e063-6294a90a7e55.zip

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
79481-004379481-0043-1

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
SODIUM BICARBONATE8MDF5V39QOIACT
TRICALCIUM PHOSPHATEK4C08XP666IACT
BENZETHONIUM CHLORIDEPH41D05744IACT
EUCALYPTUS OIL2R04ONI662IACT
PEPPERMINT OILAV092KU4JHIACT
STARCH, CORNO8232NY3SJIACT
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
Meijer Medicated Foot PowderMENTHOLMeijer Distribution07ec6c20-73c4-e5e4-e063-6294a90a7e552024-07-29WarningsExact identifier
ndc (package): 79481-0043-1
ndc (product): 79481-0043
ndc11 (package): 79481004301
spl id: 1e64f4da-93c2-0037-e063-6394a90a8750
spl set id: 07ec6c20-73c4-e5e4-e063-6294a90a7e55

Reported adverse events (FAERS/openFDA)#

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