FDA label f49967e5-ad7f-4c2b-e053-2995a90aed72

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
f4997bc5-8606-4c29-e053-2995a90a491d
SPL ID
f49967e5-ad7f-4c2b-e053-2995a90aed72
Version
1
Effective date
2023-02-13
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 07:01:30

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 Use only as directed. For external use only. When using this product: avoid contact with eyes and mucous membranes do not apply to wounds or damaged skin do not bandage tightly or use with a heating pad, other ointments, creams, sprays, or liniments. Stop use and ask doctor if: condition worsens symptoms persist for more than 7 days, or clear up and reoccur again within a few days. If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. If accidentally ingested, get medical help or contact Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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