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
2026-09-28
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/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:41:27

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 | 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.