FDA label 0eb2e8d0-0969-79d6-e063-6294a90ab274

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
0b5bf195-0ec6-4860-aa2f-ccd6f3f394ee
SPL ID
0eb2e8d0-0969-79d6-e063-6294a90ab274
Version
10
Effective date
2024-01-11
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 05:25:13

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

WARNING: FOR EXTERNAL USE ONLY. DO NOT USE IF YOU HAVE AN ALLERGY OR HYPERSENSITIVITY TO THE COMPONENTS OF THE FORMULA OR IF YOU HAVE HAD PRIOR REACTION TO THIS SALVE, STOP USE AND ASK A DOCTOR IF SYMPTOMS PERSIST OR WORSEN. AVOID CONTACT WITH EYES.

Reported adverse events (FAERS/openFDA)#

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