FDA label a25da9ed-2464-435f-be97-c87e26548f79

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
5c5140fa-f1a2-4db6-999b-ffecf692e81a
SPL ID
a25da9ed-2464-435f-be97-c87e26548f79
Version
1
Effective date
2013-11-21
Source export date
2026-09-28
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/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:13:25

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 apply to wounds, broken or damaged skin apply over large areas of the body use if you have an allergy or hypersensitivity to the components of this formula When using this product avoid contact with eyes, mouth, nose or mucous membranes. Ask a doctor before use if you are under a doctor's care for any serious condition taking any other drug Stop use and ask a doctor if skin irritation occurs. If pregnant or breast feeding, ask a health professional before use. Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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