Maximum Strength Medicated Foot Powder

Manufacturer
Jell Pharmaceuticals Pvt. Ltd. | Jell Pharmaceuticals Pvt Ltd.
Effective date
2024-12-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:44:58

Label at a glance#

ProductMaximum Strength Medicated Foot Powder
Active ingredientMENTHOL
Label structure7 sections

Dosage and administration

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 1.0%

​Purpose

OTC - PURPOSE SECTION

External analgesic

​Use

INDICATIONS & USAGE SECTION

for the temporary relief of pain and itching 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 and consult a doctor if

OTC - ASK DOCTOR SECTION

  • conditions worsens
  • redness, irritation, swelling or pain persist 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

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

​Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

benzethonium chloride, eucalyptus oil, peppermint oil, sodium bicarbonate, tricalcium phosphate, Zea mays (corn) starch

Maximum Strength Medicated Foot Powder

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
30400-507-01Maximum Strength Medicated Foot Powder283 g in 1 BOTTLE, PLASTICPOWDER2832

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
30400-507MAXIMUM STRENGTH MEDICATED FOOT POWDER (MEDICATED FOOT POWDER) POWDER [JELL PHARMACEUTICALS PVT. LTD.]2Current NDC, Legacy NDC, 1 package rows20241220_cdaae985-5363-e9d2-e053-2995a90a2682.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
30400-50730400-507-01

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#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated 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 PowderMEDICATED FOOT POWDERJell Pharmaceuticals Pvt. Ltd.cdaae985-5363-e9d2-e053-2995a90a26822024-12-18WarningsExact identifier
ndc (package): 30400-507-01
ndc (product): 30400-507
ndc11 (package): 30400050701
spl id: 2987d192-5ee3-c6df-e063-6294a90a1b77
spl set id: cdaae985-5363-e9d2-e053-2995a90a2682