FDA label 803c5939-1c76-49d2-ad56-7ecf35fdd931

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: 45009b14-3128-480c-9169-b6dcba7ed3fb
SPL ID: 803c5939-1c76-49d2-ad56-7ecf35fdd931
Version: 4
Effective date: 2015-07-13
Source export date: 2026-10-12
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/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:42:43

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		803c5939-1c76-49d2-ad56-7ecf35fdd931	id
spl set id		45009b14-3128-480c-9169-b6dcba7ed3fb	set_id

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

Adverse reactions sections page 1 of 1 · 1 matching rows.

ADVERSE REACTIONS Allergic sensitization has been reported following both oral and parenteral administration of folic acid.

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