FDA label 1e63a206-a0f1-79e6-e063-6294a90aeab4

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
0171c71c-4f02-4917-e063-6394a90a6d6e
SPL ID
1e63a206-a0f1-79e6-e063-6294a90aeab4
Version
2
Effective date
2024-07-29
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:39:14

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 Do not use the product to areas with scars, eczema, or dermatitis. Ask a doctor or pharmacist before use if you are In later stage of pregnancy. When using this product • this product is for external use only • this product is not suitable for children under 3 years of age • keep out of direct sunlight Stop use and ask a doctor if irritation, rash, red spots on skin, or swelling occurs. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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