FDA label 350356ca-ffa8-4312-ac0f-b74cb5203932

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: e8e67c0b-90ec-4eeb-b7d8-b54531521caa
SPL ID: 350356ca-ffa8-4312-ac0f-b74cb5203932
Version: 7
Effective date: 2013-08-23
Source export date: 2026-11-06
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/5731a8c92e1c0dd2a09d2f92b410e7a70ea29cbf6b8040a6a05e4be5b7c51f0d/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:41:19

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		350356ca-ffa8-4312-ac0f-b74cb5203932	id
spl set id		e8e67c0b-90ec-4eeb-b7d8-b54531521caa	set_id

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

Warnings Do not use • if you are taking mineral oil • for longer than one week • when abdominal pain, nausea or vomiting are present

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