FDA label 2c213b07-50ea-46f6-84f8-98d8ca4b7c16

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
2f15509a-487e-6db8-e054-00144ff88e88
SPL ID
2c213b07-50ea-46f6-84f8-98d8ca4b7c16
Version
4
Effective date
2017-04-11
Source export date
2026-10-12
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:29:24

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.