FDA label 4603c1ef-bf2f-42e8-9b25-92c1abdfe0f5

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
7623ee24-f0fe-498c-aca3-4ff4e5c7cdc3
SPL ID
4603c1ef-bf2f-42e8-9b25-92c1abdfe0f5
Version
1
Effective date
2015-08-06
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 05:21:59

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 Warnings: 1. Stop using the product if the following problems arise while using the product as continued use could worsen the symptoms; consult with a dermatologist. 2. Do not use on areas with wounds, eczema, and dermatitis. 3. Storage and handling precautions. 4. Wash off the product if it gets in the eye. 5. Inadequate cleansing after use could lead to bleaching; cleanse adequately after use. 6. Keep out of reach of children. 7. Store in a cool, dry place away from direct sunlight. 8. External use only.

Reported adverse events (FAERS/openFDA)#

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