FDA label f05a1679-1319-7e73-e053-2a95a90a905a

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
1469366a-5e93-4a2c-96b6-425b1cc7b2d9
SPL ID
f05a1679-1319-7e73-e053-2a95a90a905a
Version
3
Effective date
2022-12-21
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:19:56

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 . Do not use otherwise than as directed. Do not use if known sensitivity to product. If pregnant or breastfeeding, ask a healthcare professional before using this product. Keep out of reach of children. Flammable. Keep away from heat and flame. When using this product Avoid contact with eyes or mouth. Stop use and ask a doctor If condition worsens, or symptoms persists for more than 7 days, symptoms do not get better, or if redness, irritation, swelling, pain or other symptoms occur or increase.

Reported adverse events (FAERS/openFDA)#

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