GUNA-ANTI IL 1

Product NDC
17089-398
11-digit product format
170890398
Labeler code
17089
Product ID
17089-398_ed853c61-ca6e-4c3d-e053-2995a90aecb9
Type
HUMAN OTC DRUG
Nonproprietary name
ANTI-INTERLEUKIN-1.ALPHA. IMMUNOGLOBULIN G RABBIT- CANAKINUMAB
Dosage form
SOLUTION/ DROPS
Route
ORAL
Labeler
Guna spa
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2008-06-17
Substance
ANTI-INTERLEUKIN-1.ALPHA. IMMUNOGLOBULIN G RABBIT; CANAKINUMAB
Active strength
4; 4 [hp_C]/30mL; [hp_C]/30mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
GUNA-ANTI IL 1
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ANTI-INTERLEUKIN-1.ALPHA. IMMUNOGLOBULIN G RABBIT4 [hp_C]/30mL
CANAKINUMAB4 [hp_C]/30mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
ML4QRZ1HCLInternal UNII lookup
37CQ2C7X93Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
aee80c48-6271-48bb-baaa-31427fef1f26Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bd1801bf-1b8e-49c6-894d-a4af5821c1abProduct name120161129

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17089-398-182020-03-13C16284748780-19d75b9d0-f08e-f424-e053-dadaa90a57ceGUNA-ANTI IL1
17089-398-182020-01-31C16284748780-19d75b9d0-f08e-f424-e053-dadaa90a57ceGUNA-ANTI IL1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17089-398-18GUNA-ANTI IL 11 in 1 BOXSOLUTION/ DROPS15
17089-398-18GUNA-ANTI IL 130 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS305

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17089-398GUNA-ANTI IL 1 (ANTI-INTERLEUKIN-1.ALPHA. IMMUNOGLOBULIN G RABBIT- CANAKINUMAB) SOLUTION/ DROPS [GUNA SPA]5Current NDC, Legacy NDC, 2 package rows20221116_aee80c48-6271-48bb-baaa-31427fef1f26.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
GUNA-ANTI IL 1ANTI-INTERLEUKIN-1.ALPHA. IMMUNOGLOBULIN G RABBIT- CANAKINUMABGuna spaaee80c48-6271-48bb-baaa-31427fef1f262022-11-15WarningsExact identifier
ndc (product): 17089-398

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
17089-398-18170890398181 BOTTLE, DROPPER in 1 BOX (17089-398-18) / 30 mL in 1 BOTTLE, DROPPER2018-12-210000-00-00NoNoCurrent