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

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 Identifiers#

Field, Values table
FieldValues
Unii9O1TT75I7L

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

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