FDA label 336045fe-7a57-2ac3-e063-6294a90a6926

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
e1ef2f77-e140-9da5-e053-2a95a90a0206
SPL ID
336045fe-7a57-2ac3-e063-6294a90a6926
Version
3
Effective date
2025-04-22
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:25:01

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

For external use only Do not: use if you have an allergy or hypersensitivity to components of the formula apply to wounds or damaged skin apply to children under two years of age When using this product: avoid contact with eyes do not bandage tightly apply over large areas of the body Stop use and ask a doctor if: condition worsens If symptoms persists for more than 7 days or clear up and again within a few days rash develops​ If swallowed get medical help of contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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