FDA label bf00fcd0-61ed-3cc3-e053-2a95a90a8e0a

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: aa7cf451-f7c3-5d01-e053-2a95a90a9a39
SPL ID: bf00fcd0-61ed-3cc3-e053-2a95a90a8e0a
Version: 2
Effective date: 2021-04-02
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 06:13:03

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		bf00fcd0-61ed-3cc3-e053-2a95a90a8e0a	id
spl set id		aa7cf451-f7c3-5d01-e053-2a95a90a9a39	set_id

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 and mucous membranes; DURATION OF USE: Consult a health care practitioner for use beyond 7 days. CAUTIONS AND WARNINGS: Call a Poison Control Center immediately if overdose or accidental ingestion occurs; Store in airtight, light-resistant container at room temperature; Stop use and consult a health care practitioner if symptoms worsen, re-occur within a few days; KNOWN ADVERSE REACTIONS: If you experience pain, swelling or blistering, stop use and get medical help right away; Stop use if hypersensitivity/allergy, rashes and/or burning discomfort occur.

Reported adverse events (FAERS/openFDA)#

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