FDA label 7bd6ba71-47fc-4858-9bcb-52137f624920

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
cbec7df1-2e60-4edf-a9d9-3b1cbd4315c3
SPL ID
7bd6ba71-47fc-4858-9bcb-52137f624920
Version
1
Effective date
2011-12-20
Source export date
2026-10-12
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/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:35:52

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. Mild irritation may be reduced by less frequent use. If excess irritation occurs, discontinue use. If irritation persists, consult a physician. Keep away from eyes, lips, mouth and nostrils. If contact occurs, rinse thoroughly with water. Using other topical acne products at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one product should be used unless directed by a health care practitioner. This product may bleach hair or dyed fabrics. Keep out of reach of children. Keep from heat.

Reported adverse events (FAERS/openFDA)#

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