FDA label d3d209ba-434c-1f9d-e053-2a95a90aaa7f

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
c2d68f95-5a57-4d7f-a7f7-8fc4dc42e9eb
SPL ID
d3d209ba-434c-1f9d-e053-2a95a90aaa7f
Version
6
Effective date
2021-12-23
Source export date
2026-09-28
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/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:02:21

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 damaged skin, on wounds, with a heating pad. Stop and ask a doctor if condition worsens, symptoms persist for more than 7 days, or clear up and occur again within a few days. When using this product avoid contact with eyes. Do not bandage tightly. Avoid inhaling dried residue from application site which may cause sneezing, nasal irritation or tearing. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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