FDA.reportPublic FDA data

FDA label 1e639851-3013-b4eb-e063-6294a90ada3a

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
0171c60a-1a15-c3ad-e063-6294a90a7262
SPL ID
1e639851-3013-b4eb-e063-6294a90ada3a
Version
3
Effective date
2024-07-29
Source export date
2026-09-28
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:14:12

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 before use if you have ■ irritation ■ rash ■ red spots on skin ■ swelling 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 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.