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
Jell Pharmaceuticals Pvt. Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
cdaae985-5363-e9d2-e053-2995a90a2682
SPL ID
2987d192-5ee3-c6df-e063-6294a90a1b77
Version
2
Effective date
2024-12-18
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:25:01
Harmonized routes table
Harmonized routes
TOPICAL

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.