FDA label b9d4f2ce-586f-4cba-a30d-96fb5c1afd0e

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
b8f8ec7d-7930-4b70-84fb-838992000409
SPL ID
b9d4f2ce-586f-4cba-a30d-96fb5c1afd0e
Version
2
Effective date
2021-06-24
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 When using this product • use only as directed • do not bandage tightly • do not use with heating pad • avoid contact with eyes and mucous membranes • do not apply to wounds, damaged, broken or irritated skin • do not use at the same time as other topical analgesics Stop use and ask a doctor if • condition worsens • redness or irritation develops • symptoms last more than 7 days or clear up and occur again within a few days • you experience burning, swelling or blistering where applied If pregnant or breast-feeding ask a healthcare professional before use. 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.