FDA.reportPublic FDA data

FDA label 6f0a625a-8fcd-4101-8d35-73343c7d2ac2

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
2359fbb2-1251-4d7d-aea8-1e9052943f16
SPL ID
6f0a625a-8fcd-4101-8d35-73343c7d2ac2
Version
1
Effective date
2020-04-08
Source export date
2026-10-12
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:23:48

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 Allergy alert: If prone to allergic reaction from herbs, consult a doctor before use. Do not use on skin with open wounds if you are allergic to the ingredients of this product if pregnant or breast-feeding When using this product avoid contact with the eyes, mouth or rashes avoid contact with hair Stop use and ask a doctor if itching, rashes and excessive skin irritation develops symptoms persist for more than 9 days symptoms become worse

Reported adverse events (FAERS/openFDA)#

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