FDA label 0cfc399e-7734-2a28-e063-6294a90a2f16

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
ad3dfa40-e33a-5087-e053-2995a90abbbc
SPL ID
0cfc399e-7734-2a28-e063-6294a90a2f16
Version
4
Effective date
2023-12-20
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:31:44

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 use only as directed Do not use with other topical products on open wounds or damaged skin Stop use and ask a doctor if condition worsens redness is present irritation develops do not apply local heat (such as heating pads) to the area of use you experience signs of skin injury, such as pain, swelling or blistering where the product was applied If pregnant or breast-feeding, ask a health professional before use. KEEP OUT OF REACH OF CHILDREN. In case of ingestion, seek professional assistance and contact poison control immediately.

Reported adverse events (FAERS/openFDA)#

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