FDA label 9046e1f3-344e-2119-e053-2a95a90a6edd

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
9046e0e6-90b0-fa51-e053-2a95a90ab89f
SPL ID
9046e1f3-344e-2119-e053-2a95a90a6edd
Version
1
Effective date
2019-08-16
Source export date
2026-11-06
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/b0d9ca61dc485ebaf55e14a76d7d677668e40ef1e1978cdbcc4d73d58eba0b99/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:49:37

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

1) Discontinue use or consult dermatologist if irritation, itching or swelling appears after applying the product. 2) Avoid applying product on the wounded, inflamed skin parts. 3) Cautions for the storage and handing a)Keep out of children. b)Avoid direct sun light c)Avoid applying around eyes

Reported adverse events (FAERS/openFDA)#

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