FDA label d57c1968-21ef-0c99-e053-2a95a90a37b6

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
a3595570-1398-31ae-e053-2995a90ae7bd
SPL ID
d57c1968-21ef-0c99-e053-2a95a90a37b6
Version
2
Effective date
2022-01-13
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:23:37

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. When using this product ■ Do not get in eyes ■ Do not apply over large areas of the body ■ In case of deep or puncture wounds, animal bites or serious burns consult a doctor. ■ Do not bandage. 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. Do not use longer than one week unless directed by doctor. Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away. If in eyes, flush with water for 15 minutes and call a physician.

Reported adverse events (FAERS/openFDA)#

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