FDA label 0c29b233-33a5-2355-e063-6294a90aa2d0

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
0c29b233-33a4-2355-e063-6294a90aa2d0
SPL ID
0c29b233-33a5-2355-e063-6294a90aa2d0
Version
1
Effective date
2023-12-10
Source export date
2026-11-06
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/d05434af5edc4383b7c7894a8f2d94df21171d17714450933cecdfc35cedfa3d/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:46:42

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 1.For sensitive skin, it is recommended to conduct an allergy test on the back of the ear before using the product. Useit if no adverse effects occur. 2.lf such abnormalities as rash, swelling,pruritus or allergic reaction occur during or after applying the product, stop using it immediately and seek medical advice.

Reported adverse events (FAERS/openFDA)#

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