FDA.reportPublic FDA data

FDA label d715d706-add6-471f-bbfa-42db129affd5

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
e94b59b1-7f18-4688-a4e3-4cc338af4f45
SPL ID
d715d706-add6-471f-bbfa-42db129affd5
Version
1
Effective date
2020-06-29
Source export date
2026-11-06
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/10387d7618367cd955339e75d48af3d11f99f789153db05c529d9fad6eccc645/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:21:25

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 | Flammable, keep away from fire or flame, heat, sparks, and sources of static discharge Do not use |In eyes | On children less than 2 years of age | On open skin wounds When using this product |If in eyes, rinse promptly and thoroughly with water | Discontinue use if irritation and redness develops Stop use and ask a doctor if skin irritation or redness occurs or persists for more than 72 hours. 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.