FDA label 98d290a3-8789-7153-e053-2a95a90ac03c

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
bc5a71df-0ea0-4d7b-bd60-dd67ece7a1c7
SPL ID
98d290a3-8789-7153-e053-2a95a90ac03c
Version
6
Effective date
2019-12-03
Source export date
2026-11-06
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:58:28

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 on wounds or damaged skin or if you are allergic to ingredients in the product. When using this product avoid contact with eyes. If product gets into eyes, rinse thoroughly with water. do not bandage tightly or use a heating pad. Stop use and ask a doctor if rash appears. condition worsens, if symptoms persist for more than 7 days, or if symptoms clear up and occur again within a few days. 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.

Reported adverse events (FAERS/openFDA)#

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