FDA label d8005abc-2f81-2d28-e053-2a95a90a45fe

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
c2b427c0-9612-7153-e053-2995a90aa6d0
SPL ID
d8005abc-2f81-2d28-e053-2a95a90a45fe
Version
6
Effective date
2022-02-14
Source export date
2026-11-06
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/b0d9ca61dc485ebaf55e14a76d7d677668e40ef1e1978cdbcc4d73d58eba0b99/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:47:35

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

For external use only. Use only as directed. Stop use and ask doctor if - Condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days. When using this product - Avoid contact with eyes - Do not apply to wounds or damaged skin - Do not bandage tightly Flammable - Keep away from fire or flame. If pregnant or breastfeeding, ask a health care professional before use. Keep out of reach of children. In case of overdose, 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.