FDA label 8eab6551-3d46-4c86-a11b-c599d9fd3301

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
1449fb0a-be6b-4d08-b3f3-cd4d027afc17
SPL ID
8eab6551-3d46-4c86-a11b-c599d9fd3301
Version
1
Effective date
2020-11-03
Source export date
2026-10-12
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:59:01

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. ​DO NOT USE ON WOUNDS OR DAMAGED SKIN. WHEN USING THIS PRODUCTS: ​AVOID BANDAGING TIGHTLY, AVOID CONTACT WITH EYES, KEEP OUT OF REACH OF CHILDREN . ​STOP USE AND ASK DOCTOR IF: CONDITION WORENS, SYMPTONS PERSIST FOR MORE THAN 7 DAYS, CLEAR UP AND OCCUR AGAIN WITHIN A FEW DAYS.

Reported adverse events (FAERS/openFDA)#

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