FDA.reportPublic FDA data

GUNA-BDNF

Manufacturer
Guna spa
Effective date
2026-06-11
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
daily-update
Hydrated at
2026-06-13 05:10:06

Label at a glance#

ProductGUNA-BDNF
Active ingredientBRAIN-DERIVED NEUROTROPHIC FACTOR HUMAN
Label structure10 sections

Dosage and administration

Take 15 minutes before meals. Adults and children 12 years and older     20 drops twice a day in a little water. Hold in the mouth for about 30 seconds then swallow. Children  between 12 years and 6 years of age     10 drops twice a day in a little water. Hold in the mouth for about 30 seconds then swallow. Children under 6 years      5 drops twice a day in a glass of water.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

BRAIN-DERIVED NEUROTROPHIC FACTOR 4C NEUROTROPHIC SUPPORT

PURPOSE

OTC - PURPOSE SECTION

Neurotrophic Support

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medicines out of reach of children

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Neurotrophic Support

WARNINGS

WARNINGS SECTION

  • Stop use and ask doctor if symptoms worsen or persist more than 5 days
  • If pregnant or breast feeding ask a doctor before use.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Take 15 minutes before meals.
Adults and children 12 years and older    20 drops twice a day in a little water. Hold in the mouth for about 30 seconds then swallow.
Children  between 12 years and 6 years of age    10 drops twice a day in a little water. Hold in the mouth for about 30 seconds then swallow.
Children under 6 years     5 drops twice a day in a glass of water.

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Ethyl Alcohol 30%

INDICATIONS & USAGE SECTION

take 15 minutes before meals

DOSAGE & ADMINISTRATION SECTION

Adults and children twelve years and older: 20 drops twice a day in a little water- Hold in the mouth for about 30 seconds then swallow.

Children between 12 years and 6 years of age: 10 drops twice a day in a little water- Hold in the mouth for about 30 seconds then swallow.

Children under 6 years: consult a physician

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5U1BDN-Rev065U1BDN-Rev06

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData Matrix5U1BDN5U1BDN-Rev06.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17089-370-182020-03-13C16284748780-19d75b9d0-9907-f424-e053-dadaa90a57ceGUNA-BDNF
17089-370-182020-03-13C16284748780-19d75b9d0-9907-f424-e053-dadaa90a57ceGUNA-BDNF
17089-370-182020-01-31C16284748780-19d75b9d0-9907-f424-e053-dadaa90a57ceGUNA-BDNF
17089-370-182020-01-31C16284748780-19d75b9d0-9907-f424-e053-dadaa90a57ceGUNA-BDNF

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BRAIN-DERIVED NEUROTROPHIC FACTOR HUMANACTIVE INGREDIENT7171WSG8A21
BRAIN-DERIVED NEUROTROPHIC FACTOR HUMANACTIVE MOIETY7171WSG8A21
ALCOHOLINACTIVE INGREDIENT3K9958V90M1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17089-37017089-370-18

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
BRAIN-DERIVED NEUROTROPHIC FACTOR HUMAN7171WSG8A2ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52022-11-15full-release2026-06-01 02:18:33

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 22 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MSOLUTION / ORAL6624 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE, EXTENDED RELEASE / ORAL8 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MTABLET, DELAYED RELEASE / ORALNAExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCONCENTRATE / ORAL198 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE / ORAL882 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / ORAL150.68 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / ORAL210 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / ORAL150.68 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MELIXIR / ORAL13675 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MTABLET, DELAYED RELEASE / ORALNAExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSYRUP / ORAL21000 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSYRUP / ORAL21000 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE / ORAL882 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MELIXIR / ORAL13675 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCONCENTRATE / ORAL198 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSUSPENSION / ORAL681 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / ORAL210 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / ORAL6624 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE, EXTENDED RELEASE / ORAL8 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSUSPENSION / ORAL681 mgExact identifier — unii+route
22 equally ranked IID candidates

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-BDNFBRAIN-DERIVED NEUROTROPHIC FACTORGuna spaa5b5bd86-691b-44d8-b412-07022fb43e542026-06-11WarningsExact identifier
ndc (package): 17089-370-18
ndc (product): 17089-370
ndc11 (package): 17089037018
spl id: 53f56240-9a13-180a-e063-6294a90afd1e
spl set id: a5b5bd86-691b-44d8-b412-07022fb43e54

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.