FDA label b403e258-34dc-f69e-e053-2a95a90ac185

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
a12ad948-2027-4495-a966-03403fb4be53
SPL ID
b403e258-34dc-f69e-e053-2a95a90ac185
Version
2
Effective date
2020-11-13
Source export date
2026-10-12
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:26:41

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 2 matching rows.

warnings

Warnings For external use only. If pregnant or breast feeding, consult a healthcare professional. Allergy Alert: If you are allergic to any ingredients of this product, ask a doctor before use.

warnings

Do not use on wounds or damaged skin with, or at the same time as, other external analgesic products. When using this product use only as directed do not bandage tightly or use with heating pad. avoid contact with the eyes and mucous membranes. Stop use and ask a doctor if conditions worsens. symptoms persist more than 7 days or clear up and occur again within a few days. rash, itiching, or excessive irritation develops. 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.