GUNA-IL 10

Product NDC
17089-388
11-digit product format
170890388
Labeler code
17089
Product ID
17089-388_ed8186ee-6e10-0c13-e053-2a95a90a8f0a
Type
HUMAN OTC DRUG
Nonproprietary name
INTERLEUKIN-10
Dosage form
SOLUTION/ DROPS
Route
ORAL
Labeler
Guna spa
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2008-06-17
Substance
INTERLEUKIN-10
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 10
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
INTERLEUKIN-104 [hp_C]/30mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
9SC4O216V9Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
d6faade4-6263-44d3-b278-12088eb56e46Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2020-03-13GUNA-IL 10
2020-03-13GUNA-IL 10
2020-01-31GUNA-IL 10
2020-01-31GUNA-IL 10

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17089-388-18GUNA-IL 101 in 1 BOXSOLUTION/ DROPS15
17089-388-18GUNA-IL 1030 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS305

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
INTERLEUKIN-10ACTIVE INGREDIENT9SC4O216V9GUNA-IL 10 (INTERLEUKIN-10) SOLUTION/ DROPS [GUNA SPA]1
INTERLEUKIN-10ACTIVE MOIETY9SC4O216V9GUNA-IL 10 (INTERLEUKIN-10) SOLUTION/ DROPS [GUNA SPA]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MGUNA-IL 10 (INTERLEUKIN-10) SOLUTION/ DROPS [GUNA SPA]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17089-388GUNA-IL 10 (INTERLEUKIN-10) SOLUTION/ DROPS [GUNA SPA]5Current NDC, Legacy NDC, 2 package rows20221116_d6faade4-6263-44d3-b278-12088eb56e46.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 10INTERLEUKIN-10Guna spad6faade4-6263-44d3-b278-12088eb56e462026-06-10WarningsExact identifier
ndc (product): 17089-388

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
17089-388-18170890388181 BOTTLE, DROPPER in 1 BOX (17089-388-18) / 30 mL in 1 BOTTLE, DROPPER2010-05-260000-00-00NoNoCurrent