FDA label f26752b8-305b-5f9e-e053-2995a90a7de0

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: 23080695-433e-4866-bb3f-90537f80b4a9
SPL ID: f26752b8-305b-5f9e-e053-2995a90a7de0
Version: 11
Effective date: 2023-01-16
Source export date: 2026-09-28
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:28:15

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		f26752b8-305b-5f9e-e053-2995a90a7de0	id
spl set id		23080695-433e-4866-bb3f-90537f80b4a9	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. When using this product Avoid contact with eyes or mucous membranes do not apply to wounds or damaged skin do not use with other ointments, creams, sprays or liniments do not apply to irritated skin or if excessive irritation develops do not bandage wash hands after use with cool water do not use with heating pad or device store in a cool dry place Stop use and ask doctor if: condition worsens, or if symptoms persist for more than 7 days, or clear up and recur. If pregnant or breast feeding: ask a health professional befgore use.

Reported adverse events (FAERS/openFDA)#

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