FDA label 05a4985f-8319-e833-e063-6294a90a094b

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
c9d78e29-f3af-89e9-e053-2a95a90a75c1
SPL ID
05a4985f-8319-e833-e063-6294a90a094b
Version
4
Effective date
2023-09-18
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 06:23:29

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 or mucous membranes▪Do not apply to wounds or damaged skin▪Do not bandage tightly▪Wash hands with cool water after use▪Do not use with heating pad or device▪Stop use and ask a doctor if you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied. Discontinue use and consult doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and recur. If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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