GUNA-ANTI IL 1

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)

Brand name: GUNA-ANTI IL 1
Generic name: ANTI-INTERLEUKIN-1.ALPHA. IMMUNOGLOBULIN G RABBIT- CANAKINUMAB
Manufacturer: Guna spa
Product type: HUMAN OTC DRUG
SPL set ID: aee80c48-6271-48bb-baaa-31427fef1f26
SPL ID: ed853c61-ca6e-4c3d-e053-2995a90aecb9
Version: 5
Effective date: 2022-11-15
Source export date: 2026-09-28
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/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:09:50

Harmonized routes table
Harmonized routes
ORAL

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		GUNA-ANTI IL 1	openfda.brand_name
generic name		ANTI-INTERLEUKIN-1.ALPHA. IMMUNOGLOBULIN G RABBIT- CANAKINUMAB	openfda.generic_name
manufacturer name		Guna spa	openfda.manufacturer_name
ndc	package	17089-398-18	openfda.package_ndc
ndc	product	17089-398	openfda.product_ndc
ndc11	package	17089039818	derived:openfda.package_ndc
spl id		ed853c61-ca6e-4c3d-e053-2995a90aecb9	id
spl set id		aee80c48-6271-48bb-baaa-31427fef1f26	set_id
unii		37CQ2C7X93	openfda.unii
unii		ML4QRZ1HCL	openfda.unii

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 Stop use and ask doctor if symptoms persist more than 5 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. Contains ethyl alcohol 30%

Reported adverse events (FAERS/openFDA)#

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