FDA label 030a7008-80d0-4d97-a85e-0207d55eb6b9

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: 12ecb20f-dc52-4d07-a75c-45ef885df69a
SPL ID: 030a7008-80d0-4d97-a85e-0207d55eb6b9
Version: 3
Effective date: 2012-03-05
Source export date: 2026-10-12
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/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:34:02

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		030a7008-80d0-4d97-a85e-0207d55eb6b9	id
spl set id		12ecb20f-dc52-4d07-a75c-45ef885df69a	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 Do not use if you ever had a rash or other allergic reaction to loperamide HCl Do Not Use if you have bloody or black stool Ask a doctor before use if you have high fever (greater than 101F) mucus present in your stool history of liver disease Ask a doctor or pharmacist before use if you are taking antibiotics Stop use and ask a doctor if diarrhea lasts for more than 2 days If pregnant or breast-feeding Ask a health professional before use. Keep out of reach of children In case of overdose, 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.