GUNA-IL 5

Product NDC
17089-383
11-digit product format
170890383
Labeler code
17089
Product ID
17089-383_7e91aab5-b2ad-c62f-e053-2991aa0ad61e
Type
HUMAN OTC DRUG
Nonproprietary name
INTERLEUKIN-5
Dosage form
SOLUTION/ DROPS
Route
ORAL
Labeler
Guna spa
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2008-06-17
Substance
INTERLEUKIN-5
Active strength
4 [hp_C]/30mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
GUNA-IL 5
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
INTERLEUKIN-54 [hp_C]/30mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
9O1TT75I7LInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
d2103cb5-40d2-4174-ab28-62df44c7fba4Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17089-383-18GUNA-IL 530 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS302
17089-383-18GUNA-IL 51 in 1 BOXSOLUTION/ DROPS12

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
INTERLEUKIN-5ACTIVE INGREDIENT9O1TT75I7LGUNA-IL 5 (INTERLEUKIN-5) SOLUTION/ DROPS [GUNA SPA]1
INTERLEUKIN-5ACTIVE MOIETY9O1TT75I7LGUNA-IL 5 (INTERLEUKIN-5) SOLUTION/ DROPS [GUNA SPA]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MGUNA-IL 5 (INTERLEUKIN-5) SOLUTION/ DROPS [GUNA SPA]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17089-383GUNA-IL 5 (INTERLEUKIN-5) SOLUTION/ DROPS [GUNA SPA]2Current NDC, Legacy NDC, 2 package rows20190104_d2103cb5-40d2-4174-ab28-62df44c7fba4.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 5INTERLEUKIN-5Guna spad2103cb5-40d2-4174-ab28-62df44c7fba42018-12-21WarningsExact identifier
ndc (product): 17089-383

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
17089-383-18170890383181 BOTTLE, DROPPER in 1 BOX (17089-383-18) / 30 mL in 1 BOTTLE, DROPPER2015-11-010000-00-00NoNoCurrent