FDA label 7dece06e-088a-dc8f-e053-2a91aa0a960f

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
54981780-1d11-4601-8f7e-c1f318a4614d
SPL ID
7dece06e-088a-dc8f-e053-2a91aa0a960f
Version
3
Effective date
2018-12-26
Source export date
2026-08-01
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/206e0852f7011b53c21719ec5c68ac6752381d0fcd1d348f7428adad64429e89/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:16:58

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 • with other topical pain relievers • with heating pads or heating devices When using this product • do not use in or near eyes • do not apply to wounds or damaged skin • do not bandage tightly Stop use and ask a doctor if • condition worsens • symptoms last more than 7 days or clear up and occur again within a few days • redness or irritation develops If pregnant or breast-feeding • ask a health professional before use Keep out of reach of children • If swallowed, get medical help or contact a Poison Control Center right away.