FDA.reportPublic FDA data

GUNA-INF GAMMA

Product NDC
17089-378
11-digit product format
170890378
Labeler code
17089
Product ID
17089-378_ed813de7-e0d5-74b9-e053-2995a90a6a73
Type
HUMAN OTC DRUG
Nonproprietary name
INTERFERON GAMMA-1B
Dosage form
SOLUTION/ DROPS
Route
ORAL
Labeler
Guna spa
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2008-06-17
Substance
INTERFERON GAMMA-1B
Active strength
4 [hp_C]/30mL
Pharmacologic classes
Interferon gamma [EPC], Interferon-gamma [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
GUNA-INF GAMMA
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
INTERFERON GAMMA-1B4 [hp_C]/30mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
21K6M2I7AGInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
a09a33a1-5c7c-493d-abc7-907edd8e97caAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d45267e3-883a-4760-85b5-ebc565c21683Product name120150910

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17089-378-182020-03-13C16284748780-19d75b9d1-23d3-f424-e053-dadaa90a57ceGUNA-INF GAMMA
17089-378-182020-01-31C16284748780-19d75b9d1-23d3-f424-e053-dadaa90a57ceGUNA-INF GAMMA

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17089-378-18GUNA-INF GAMMA30 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS305
17089-378-18GUNA-INF GAMMA1 in 1 BOXSOLUTION/ DROPS15

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
INTERFERON GAMMA-1BACTIVE INGREDIENT21K6M2I7AGGUNA-INF GAMMA (INTERFERON GAMMA-1B) SOLUTION/ DROPS [GUNA SPA]1
INTERFERON GAMMA-1BACTIVE MOIETY21K6M2I7AGGUNA-INF GAMMA (INTERFERON GAMMA-1B) SOLUTION/ DROPS [GUNA SPA]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MGUNA-INF GAMMA (INTERFERON GAMMA-1B) SOLUTION/ DROPS [GUNA SPA]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17089-378GUNA-INF GAMMA (INTERFERON GAMMA-1B) SOLUTION/ DROPS [GUNA SPA]5Current NDC, Legacy NDC, 2 package rows20221116_a09a33a1-5c7c-493d-abc7-907edd8e97ca.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-INF GAMMAINTERFERON GAMMA-1BGuna spaa09a33a1-5c7c-493d-abc7-907edd8e97ca2022-11-15WarningsExact identifier
ndc (product): 17089-378

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
17089-378-18170890378181 BOTTLE, DROPPER in 1 BOX (17089-378-18) / 30 mL in 1 BOTTLE, DROPPER2008-06-170000-00-00NoNoCurrent