FDA label 6a1b3823-7b1f-4c28-b74d-889ccd7b3703

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: 5797b7b0-d5b2-41da-9825-245cc9b6f348
SPL ID: 6a1b3823-7b1f-4c28-b74d-889ccd7b3703
Version: 2
Effective date: 2024-11-15
Source export date: 2026-10-12
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:10:28

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		6a1b3823-7b1f-4c28-b74d-889ccd7b3703	id
spl set id		5797b7b0-d5b2-41da-9825-245cc9b6f348	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 Stop use and consult a doctor in case of bleeding Do not exceed recommended daily dosage unless directed by a doctor. • if condition worsens or does not improve within 7 days. Do not put product into rectum by using fingers or any mechanical device or applicator Allergy Alert: Certain persons can develop allergic reactions to this product. If the symptoms being treated does not subside or if redness, ittitation, swelling, pain or other symptoms develop or increase, discontinue use and consult a doctor. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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