FDA.reportPublic FDA data

GUNA-IL 2

Product NDC
17089-380
11-digit product format
170890380
Labeler code
17089
Product ID
17089-380_ed8137f8-9931-234c-e053-2a95a90a5769
Type
HUMAN OTC DRUG
Nonproprietary name
ALDESLEUKIN
Dosage form
SOLUTION/ DROPS
Route
ORAL
Labeler
Guna spa
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2008-06-17
Substance
ALDESLEUKIN
Active strength
4 [hp_C]/30mL
Pharmacologic classes
Increased Lymphocyte Activation [PE], Increased Lymphocyte Cell Production [PE], Interleukin-2 [CS], Lymphocyte Growth Factor [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
GUNA-IL 2
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALDESLEUKIN4 [hp_C]/30mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
M89N0Q7EQRInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
0619f291-207a-4e01-96bd-b882726665e2Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17089-380-182020-03-13C16284748780-19d75b9d0-f937-f424-e053-dadaa90a57ceGUNA-IL 2
17089-380-182020-01-31C16284748780-19d75b9d0-f937-f424-e053-dadaa90a57ceGUNA-IL 2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17089-380-18GUNA-IL 21 in 1 BOXSOLUTION/ DROPS15
17089-380-18GUNA-IL 230 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS305

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALDESLEUKINACTIVE INGREDIENTM89N0Q7EQRGUNA-IL 2 (ALDESLEUKIN) SOLUTION/ DROPS [GUNA SPA]1
ALDESLEUKINACTIVE MOIETYM89N0Q7EQRGUNA-IL 2 (ALDESLEUKIN) SOLUTION/ DROPS [GUNA SPA]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MGUNA-IL 2 (ALDESLEUKIN) SOLUTION/ DROPS [GUNA SPA]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17089-380GUNA-IL 2 (ALDESLEUKIN) SOLUTION/ DROPS [GUNA SPA]5Current NDC, Legacy NDC, 2 package rows20221116_0619f291-207a-4e01-96bd-b882726665e2.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-IL 2ALDESLEUKINGuna spa0619f291-207a-4e01-96bd-b882726665e22022-11-15WarningsExact identifier
ndc (product): 17089-380

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
17089-380-18170890380181 BOTTLE, DROPPER in 1 BOX (17089-380-18) / 30 mL in 1 BOTTLE, DROPPER2010-10-060000-00-00NoNoCurrent