GUNA-IL 3

Product NDC: 17089-381
11-digit product format: 170890381
Labeler code: 17089
Product ID: 17089-381_ed819152-2967-22be-e053-2a95a90a33f6
Type: HUMAN OTC DRUG
Nonproprietary name: INTERLEUKIN-3
Dosage form: SOLUTION/ DROPS
Route: ORAL
Labeler: Guna spa
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2008-06-17
Substance: INTERLEUKIN-3
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 3
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
INTERLEUKIN-3	4 [hp_C]/30mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
VPB6TR49WU	Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
5be3096f-9046-457c-b7ba-767ffe74c07a	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
17089-381-18	2020-03-13	C162847	48780-1	9d75b9d0-74e0-f424-e053-dadaa90a57ce	GUNA-IL 3
17089-381-18	2020-01-31	C162847	48780-1	9d75b9d0-74e0-f424-e053-dadaa90a57ce	GUNA-IL 3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
17089-381-18	GUNA-IL 3	1 in 1 BOX	SOLUTION/ DROPS	1		5
17089-381-18	GUNA-IL 3	30 mL in 1 BOTTLE, DROPPER	SOLUTION/ DROPS	30		5

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
INTERLEUKIN-3	ACTIVE INGREDIENT	A802907MI4	GUNA-IL 3 (INTERLEUKIN-3) SOLUTION/ DROPS [GUNA SPA]	1
INTERLEUKIN-3	ACTIVE MOIETY	A802907MI4	GUNA-IL 3 (INTERLEUKIN-3) SOLUTION/ DROPS [GUNA SPA]	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	GUNA-IL 3 (INTERLEUKIN-3) SOLUTION/ DROPS [GUNA SPA]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
17089-381	GUNA-IL 3 (INTERLEUKIN-3) SOLUTION/ DROPS [GUNA SPA]	5	Current NDC, Legacy NDC, 2 package rows	20221116_5be3096f-9046-457c-b7ba-767ffe74c07a.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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
GUNA-IL 3	INTERLEUKIN-3	Guna spa	5be3096f-9046-457c-b7ba-767ffe74c07a	2022-11-15	Warnings	Exact identifier ndc (product): 17089-381

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
17089-381-18	17089038118	1 BOTTLE, DROPPER in 1 BOX (17089-381-18) / 30 mL in 1 BOTTLE, DROPPER	2010-05-27	0000-00-00	No	No	Current