FDA label 77cd21f8-ad73-07fa-e053-2a91aa0a44f6

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
5a92a956-c001-3d14-e053-2a91aa0af839
SPL ID
77cd21f8-ad73-07fa-e053-2a91aa0a44f6
Version
6
Effective date
2018-10-09
Source export date
2026-11-06
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/2233cb6af8c6b55a5e4a05449e8db0d2f259f3c061d5d001b654a8bea1cc1db2/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:57:09

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: On wounds or damaged skin with a heating pad ASK A DOCTOR BEFORE USE IF: You have redness over the affected area Conditions worsen or sypmtoms persist for more than 7 days Symptons clear up and occur again within a few days Excessive skin irritation occurs You are pregnant or breast feeding

Reported adverse events (FAERS/openFDA)#

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