FDA label 6cc082b1-ae18-49ed-a51b-d1c5c28792ee

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
35abbfe2-39a3-4f24-b23e-84d8614e07e7
SPL ID
6cc082b1-ae18-49ed-a51b-d1c5c28792ee
Version
1
Effective date
2010-10-18
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 06:11:01

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; avoid contact with eyes When using this product, do not; - heat - microwave - add to hot water or any container where heating water may cause splattering and result in burns - use in eyes or directly on mucous membranes take by mouth or place in nostrils - apply to wounds or damaged skin - bandage skin Consult a doctor and discontinue use: If condition worsens, persists for more than 1 week or tends to recur. Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center Immediately.

Reported adverse events (FAERS/openFDA)#

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