FDA label 85eeb5dc-2eb1-42e1-91ee-5a9278d678ac

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: c182e00b-9bb0-4af8-bc35-ee8eeda6ab18
SPL ID: 85eeb5dc-2eb1-42e1-91ee-5a9278d678ac
Version: 2
Effective date: 2024-05-22
Source export date: 2026-11-06
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/2026-11-06/bbdc0a42bf44145a63c3752991067bece7e2a518be6cc14943d33c4987faa012/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:12:20

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		85eeb5dc-2eb1-42e1-91ee-5a9278d678ac	id
spl set id		c182e00b-9bb0-4af8-bc35-ee8eeda6ab18	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 Allergy alert: Do not use if you are allergic to ranitidine or other acid reducers

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