FDA label 0bbb46ec-3020-17bb-e063-6294a90af97f

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
0bbb46ec-301f-17bb-e063-6294a90af97f
SPL ID
0bbb46ec-3020-17bb-e063-6294a90af97f
Version
1
Effective date
2023-12-04
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:24:46

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. This product is for external use. It is forbidden to take orally. 2. This product is contraindicated for pregnant women, people allergic to this product and people with allergic constitution. 3.This product is forbidden to be used on the skin with ulceration and damage. 4. This product is a health care product and is not a substitute for any medication or medical instrument.

Reported adverse events (FAERS/openFDA)#

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