FDA label 070ebef6-d635-4b23-a4ce-b430217aef1c

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: cee0edef-133f-404e-ba69-e14b602979c2
SPL ID: 070ebef6-d635-4b23-a4ce-b430217aef1c
Version: 4
Effective date: 2016-02-22
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 06:10:57

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		070ebef6-d635-4b23-a4ce-b430217aef1c	id
spl set id		cee0edef-133f-404e-ba69-e14b602979c2	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. If swallowed, contact a doctor or poison control center immediately. Keep out of the reach of children. Flammable, keep away from open flame. DO NOT USE: In the eyes If you are allergic to any of the ingredients On raw surfaces, blistered areas, or over large areas of the body WHEN USING THIS PRODUCT: Avoid contact with eyes or mucous membranes STOP USE AND ASK A DOCTOR IF: Conditions worsen clear up and then recur The condition persists for more than 7 days A rash, allergic reaction, swelling, irritation or infection occur

Reported adverse events (FAERS/openFDA)#

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