FDA.reportPublic FDA data

GUNA-IL 11

Product NDC
17089-389
11-digit product format
170890389
Labeler code
17089
Product ID
17089-389_ed81a1dd-c087-49a5-e053-2995a90aad04
Type
HUMAN OTC DRUG
Nonproprietary name
INTERLEUKIN-11
Dosage form
SOLUTION/ DROPS
Route
ORAL
Labeler
Guna spa
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2008-06-17
Substance
INTERLEUKIN-11
Active strength
4 [hp_C]/30mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

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

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
GUNA-IL 11INTERLEUKIN-11Guna spa2bceda80-56e9-40d9-9dfc-336deb6ec0552022-11-15WarningsExact identifier
ndc (product): 17089-389

Additional Listing Data#

Finished product
Yes
Brand name base
GUNA-IL 11
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
INTERLEUKIN-114 [hp_C]/30mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
O14Q7A13PTInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
2bceda80-56e9-40d9-9dfc-336deb6ec055Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17089-389-182020-03-13C16284748780-19d75b9d0-1ca8-f424-e053-dadaa90a57ceGUNA- IL 11
17089-389-182020-01-31C16284748780-19d75b9d0-1ca8-f424-e053-dadaa90a57ceGUNA- IL 11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17089-389-18GUNA-IL 1130 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS305
17089-389-18GUNA-IL 111 in 1 BOXSOLUTION/ DROPS15

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
INTERLEUKIN-11ACTIVE INGREDIENTO14Q7A13PTGUNA-IL 11 (INTERLEUKIN-11) SOLUTION/ DROPS [GUNA SPA]1
INTERLEUKIN-11ACTIVE MOIETYO14Q7A13PTGUNA-IL 11 (INTERLEUKIN-11) SOLUTION/ DROPS [GUNA SPA]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MGUNA-IL 11 (INTERLEUKIN-11) SOLUTION/ DROPS [GUNA SPA]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17089-389GUNA-IL 11 (INTERLEUKIN-11) SOLUTION/ DROPS [GUNA SPA]5Current NDC, Legacy NDC, 2 package rows20221116_2bceda80-56e9-40d9-9dfc-336deb6ec055.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
17089-389-18170890389181 BOTTLE, DROPPER in 1 BOX (17089-389-18) / 30 mL in 1 BOTTLE, DROPPER2018-12-210000-00-00NoNoCurrent