FDA label 57d4664d-0fcd-1915-e053-2991aa0a9520

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
2f9fe0b9-31ff-166b-e054-00144ff88e88
SPL ID
57d4664d-0fcd-1915-e053-2991aa0a9520
Version
2
Effective date
2017-08-28
Source export date
2026-09-28
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:13:07

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

1. If any of the following symptoms appear on the area where the product was applied, stop using the product immediately and consult a specialist. A. Several skin conditions including rash, swelling, irritation, and stimulation B. When above symptoms occur while sun rays are applied 2. Do NOT use on the area with scars, eczema or dermatitis 3. Storage and dealings warnings. A. Close tight after use B. Keep out of reach of children C. Do not keep the product in high or low temperature and keep out of sun

Reported adverse events (FAERS/openFDA)#

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