Home FDA labels 350b8fbb-d869-9503-e063-6394a90a9eb8 Dr. Canuso foot repair serum 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 Dr. Canuso foot repair serum
Generic name TOLNAFTATE SERUM
Manufacturer Renu Laboratories, LLC
Product type HUMAN OTC DRUG
SPL set ID 1fcc52c5-7030-13cb-e054-00144ff8d46c
SPL ID 350b8fbb-d869-9503-e063-6394a90a9eb8
Version 17
Effective date 2025-05-13
Source export date 2026-09-28
Source partition 13
Source file https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:37:24 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.
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 When using this product Do not use on children under 2 years of age unless directed by a doctor Avoid contact with eyes If irritation occurs, discontinue use and consult a doctor If swallowed, get medical help or consult a poison control center immediately
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.