FDA label 80171f3b-d5c9-499f-9493-aff89e777490

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: 34af91bb-e04b-d252-e063-6294a90aaf96
SPL ID: 80171f3b-d5c9-499f-9493-aff89e777490
Version: 4
Effective date: 2025-05-20
Source export date: 2026-10-12
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:56:53

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		80171f3b-d5c9-499f-9493-aff89e777490	id
spl set id		34af91bb-e04b-d252-e063-6294a90aaf96	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

For external use only. Do not use: On irritated skin or any area that is infected or reddened If allergic to any of the ingredients. If pregnant or breastfeeding, unless directed by a doctor. Avoid contact with eyes Stop use and ask a doctor if: discomfort, burning, or irritation occurs lf no improvement within 4 weeks Do not use: If pregnant or breastfeeding, unless directed by a doctor. Keep out of reach of children. If product gets intoeyes,flush with water for 15 minutes. 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.