FDA label 976434f8-b77d-a84e-e053-2995a90a5043

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)

SPL set ID
aed9fa91-1d21-4da4-8965-ea0011074ba1
SPL ID
976434f8-b77d-a84e-e053-2995a90a5043
Version
2
Effective date
2019-11-15
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 06:22:54

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 topical use only. Avoid contact with eyes and mucuos membranes. Do not use on broken skin. Strong floral aroma. Discontinue use if skin irritation develops. Shooting, burning pain in the toes and hands can be signs of diabetic neuropathy. See a health care professional on a regular basis if you are diabetic, or if you suspect you are diabetic. Keep out of reach of children. When using this product Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately. If pregnant or breast-feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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