FDA.reportPublic FDA data

GUNA-FGF

Product NDC
17089-373
11-digit product format
170890373
Labeler code
17089
Product ID
17089-373_ed812047-a685-5f21-e053-2a95a90a2019
Type
HUMAN OTC DRUG
Nonproprietary name
FIBROBLAST GROWTH FACTOR
Dosage form
SOLUTION/ DROPS
Route
ORAL
Labeler
Guna spa
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2011-03-31
Substance
VELAFERMIN
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-FGF
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
VELAFERMIN4 [hp_C]/30mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
6Z25C35927Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
c6beb454-5661-4d85-a6ba-b1971eda8965Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17089-373-18GUNA-FGF30 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS305
17089-373-18GUNA-FGF1 in 1 BOXSOLUTION/ DROPS15

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
VELAFERMINACTIVE INGREDIENT6Z25C35927GUNA-FGF (FIBROBLAST GROWTH FACTOR) SOLUTION/ DROPS [GUNA SPA]1
VELAFERMINACTIVE MOIETY6Z25C35927GUNA-FGF (FIBROBLAST GROWTH FACTOR) SOLUTION/ DROPS [GUNA SPA]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MGUNA-FGF (FIBROBLAST GROWTH FACTOR) SOLUTION/ DROPS [GUNA SPA]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17089-373GUNA-FGF (FIBROBLAST GROWTH FACTOR) SOLUTION/ DROPS [GUNA SPA]5Current NDC, Legacy NDC, 2 package rows20221116_c6beb454-5661-4d85-a6ba-b1971eda8965.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-FGFFIBROBLAST GROWTH FACTORGuna spac6beb454-5661-4d85-a6ba-b1971eda89652026-06-11WarningsExact identifier
ndc (product): 17089-373

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
17089-373-18170890373181 BOTTLE, DROPPER in 1 BOX (17089-373-18) / 30 mL in 1 BOTTLE, DROPPER2011-03-310000-00-00NoNoCurrent