Bonogen Activator

Manufacturer
Bonogen Co., Ltd
Effective date
2010-04-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:24:24

Label at a glance#

ProductBonogen Activator hair loss treatment
Active ingredientBIOTIN
Label structure2 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Biotin

DESCRIPTION SECTION

* Bonogen Activator (Hair Loss Treatment) *

1) Name of Product : Bonogen Activator (Hair Loss Treatment)
2) Caution :
· Stop using and see a doctor if any hypersensitivity symptom continues.
· Avoid storing under direct sun light or high temperature.
3) Effect :
· Provides an excellent tonic effect and prevents hair-loss.
· Increases hair longevity through palpation of cell metabolism.
4) Using method :
· Spray Bonogen Activator on the scalp 2~3 times daily as needed.
Recommendable to apply Bonogen Activator enough on the scalp prior
to going to bed.
5) Shelf life : 36 months

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

carton label
carton label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1044988biotin 0.002 % Topical SolutionPSN1
1044988biotin 0.02 MG/ML Topical SolutionSCD1
1044988biotin 0.002 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50653-3001-12019-10-21C16284748780-1956f9ecf-c96c-621f-e053-dbdaa90a74adDrug Facts
50653-3001-22019-10-21C16284748780-1956f9ecf-c96c-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50653-3001-1Bonogen Activatorhair loss treatment100 mL in 1 BOTTLE, WITH APPLICATORLIQUID1001
50653-3001-2Bonogen Activatorhair loss treatment150 mL in 1 BOTTLE, WITH APPLICATORLIQUID1501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50653-3001BONOGEN ACTIVATOR HAIR LOSS TREATMENT (BIOTIN) LIQUID [BONOGEN CO., LTD]1Legacy NDC, 2 package rows20100505_4a455987-e6bf-4794-89ba-147d5d4834b2.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BIOTINACTIVE INGREDIENT6SO6U10H041
BIOTINACTIVE MOIETY6SO6U10H041

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50653-300150653-3001-1, 50653-3001-2

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
BIOTIN6SO6U10H04ACTIB

Source Document#

Source XML

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
ff548e74-db58-404e-be2b-1d85db7984674a455987-e6bf-4794-89ba-147d5d4834b22010-04-25Exact identifier
spl id: ff548e74-db58-404e-be2b-1d85db798467
spl set id: 4a455987-e6bf-4794-89ba-147d5d4834b2

Reported adverse events (FAERS/openFDA)#

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