FDA label 24800923-5712-c9d9-e063-6394a90ac12f

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
24800923-5711-c9d9-e063-6394a90ac12f
SPL ID
24800923-5712-c9d9-e063-6394a90ac12f
Version
1
Effective date
2024-10-15
Source export date
2026-10-12
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/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:54:03

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

Warning 1: For external use only, avoid directcontact with eyes. if there is any discomfort, stop using and rinse with plenty ofwater. In severe cases, seekmedical attention promptly. 2: After use, please thoroughly cleanyour hands. This product is not allowed to be used on damaged skin. 3: Not suitable for children, pregnantor breastfeeding populations. 4: Store in a cool and dry place,avoiding direct sunlight. 5: This product may cause allergicreactions to a small number of peopleIf you feel unwell, please stop using it immediately

Reported adverse events (FAERS/openFDA)#

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