FDA label d9b5473e-a5e3-3a3b-e053-2a95a90a5d73

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
edbde739-70ef-4bb5-b109-6afead84c5ed
SPL ID
d9b5473e-a5e3-3a3b-e053-2a95a90a5d73
Version
7
Effective date
2022-03-08
Source export date
2026-10-12
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:29:11

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. Use only on the advice of a physician. Do not use On broken or irritated skin. On children under 12 years of age. If you are pregnant or nursing unless instructed by a physician. Allergy alert: Contains Sodium Metabisulfite. Sunburn alert: Limit sun exposure during treatment by using protective clothing or a sunscreen protective agent to avoid re-darkening of the skin. When using this product A mild transient stinging may occur for people with sensitive skin. Gradual lightening of the discolored area can be expected in most cases. Avoid contact with eyes and mucous membranes. In case of contact, rinse thoroughly with water. Stop using this product If irritation or rash occurs. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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