FDA label 75dc31bc-4d3f-482d-abd3-d60cdddcf89d

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
ffb0097e-eeca-4b89-9a11-975091255e5a
SPL ID
75dc31bc-4d3f-482d-abd3-d60cdddcf89d
Version
1
Effective date
2010-10-19
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:21:32

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. Do not use on broken skin. large areas of the body. When using this product, Apply to affected areas only avoid unnecessary sun exposure and use a sunscreen avoid contact with eyes/eye area, lips, mouth and nostrils. If contact occurs, rinse thoroughly with water. This product may bleach hair or dyed fabrics. Using other topical acne drugs at the same time or right after use of this product may increase dryness or irritation of the skin. Only one drug should be used unless directed by a doctor. Stop use and ask a doctor if too much skin irritation or sensitivity develops or increases. If swallowed, seek medical assistance or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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