FDA.reportPublic FDA data

GUNA-IL 4

Product NDC
17089-382
11-digit product format
170890382
Labeler code
17089
Product ID
17089-382_ed819152-2968-22be-e053-2a95a90a33f6
Type
HUMAN OTC DRUG
Nonproprietary name
BINETRAKIN
Dosage form
SOLUTION/ DROPS
Route
ORAL
Labeler
Guna spa
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2008-06-17
Substance
BINETRAKIN
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 4
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BINETRAKIN4 [hp_C]/30mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
751635Z921Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
da1f5fe8-508d-4911-804a-8489ca97e071Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2020-03-13GUNA-IL 4
2020-03-13GUNA-IL 4
2020-01-31GUNA-IL 4
2020-01-31GUNA-IL 4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17089-382-18GUNA-IL 430 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS305
17089-382-18GUNA-IL 41 in 1 BOXSOLUTION/ DROPS15

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BINETRAKINACTIVE INGREDIENT751635Z921GUNA-IL 4 (BINETRAKIN) SOLUTION/ DROPS [GUNA SPA]1
BINETRAKINACTIVE MOIETY751635Z921GUNA-IL 4 (BINETRAKIN) SOLUTION/ DROPS [GUNA SPA]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MGUNA-IL 4 (BINETRAKIN) SOLUTION/ DROPS [GUNA SPA]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17089-382GUNA-IL 4 (BINETRAKIN) SOLUTION/ DROPS [GUNA SPA]5Current NDC, Legacy NDC, 2 package rows20221116_da1f5fe8-508d-4911-804a-8489ca97e071.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 4BINETRAKINGuna spada1f5fe8-508d-4911-804a-8489ca97e0712026-06-10WarningsExact identifier
ndc (product): 17089-382

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
17089-382-18170890382181 BOTTLE, DROPPER in 1 BOX (17089-382-18) / 30 mL in 1 BOTTLE, DROPPER2008-06-170000-00-00NoNoCurrent