FDA label f1a78e10-4dc2-13b2-e053-2995a90afe7b

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
7c9f2e53-332e-4c48-83c2-8444d1afa8d3
SPL ID
f1a78e10-4dc2-13b2-e053-2995a90afe7b
Version
5
Effective date
2023-01-07
Source export date
2026-09-28
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/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:30:06

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 damaged, broken, or irritated skin with a heating pad immediately before or after taking a bath or shower Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days skin irritation occurs When using this product avoid contact with lips, eyes, nose and any mucous membranes at all times do not bandage tightly Keep out of reach of children. If swallowed get medical help or contact Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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