FDA label d60a3e9d-e881-3b19-e053-2995a90a3e8d

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
0d988182-d435-465d-b99b-5eeee7b76e74
SPL ID
d60a3e9d-e881-3b19-e053-2995a90a3e8d
Version
4
Effective date
2022-01-20
Source export date
2026-08-01
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/2026-08-01/d245bd7ce31d1d8ed63276109973402ece6c44860774da30f25b731cd7418983/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:35:27

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 WARNINGS: For external use only. When using this product: Discontinue use if excessive irritation of the skin develops. Avoid contact with eyes and mucus membranes. Do not bandage tightly. Do not use with heating pad. Stop use and ask a doctor if: ▪ Condition worsens. ▪ Severe skin irritation occurs. ▪ Pain persists for more than seven days. ▪ Pain clears up and the recurs within a few days. If pregnant or breast-feeding, ask a health care professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control immediately.