Maximum Strength Medicated Foot Powder

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Maximum Strength Medicated Foot Powder
Generic name: MEDICATED FOOT POWDER
Manufacturer: Walmart Stores Inc
Product type: HUMAN OTC DRUG
SPL set ID: b0794d48-eb8b-55c9-e053-2995a90a5b38
SPL ID: 46f6ba22-d323-2610-e063-6394a90a486a
Version: 4
Effective date: 2025-12-27
Source export date: 2026-11-06
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/97001096994db9ca8cee114e6c3bb5298d3c573158ffc1ab8692d82e76a3eb40/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 06:55:29

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Maximum Strength Medicated Foot Powder	openfda.brand_name
generic name		MEDICATED FOOT POWDER	openfda.generic_name
manufacturer name		Walmart Stores Inc	openfda.manufacturer_name
ndc	package	49035-795-01	openfda.package_ndc
ndc	product	49035-795	openfda.product_ndc
ndc11	package	49035079501	derived:openfda.package_ndc
rxcui		259579	openfda.rxcui
spl id		46f6ba22-d323-2610-e063-6394a90a486a	id
spl set id		b0794d48-eb8b-55c9-e053-2995a90a5b38	set_id
unii		L7T10EIP3A	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. When using this product avoid contact with eyes. Not for genital area Stop and consult a doctor if 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. In case of accidental ingestion, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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