Bonogen Activator
- Product NDC
- 50653-3001
- 11-digit product format
- 506533001
- Labeler code
- 50653
- Product ID
- 50653-3001_ff548e74-db58-404e-be2b-1d85db798467
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BIOTIN
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Bonogen Co., Ltd
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2010-04-25
- Marketing end
- 0000-00-00
- Substance
- BIOTIN
- Active strength
- 0 mL/mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50653-3001-1 | Bonogen Activatorhair loss treatment | 100 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 100 | | 1 |
| 50653-3001-2 | Bonogen Activatorhair loss treatment | 150 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 150 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50653-3001 | BONOGEN ACTIVATOR HAIR LOSS TREATMENT (BIOTIN) LIQUID [BONOGEN CO., LTD] | 1 | Legacy NDC, 2 package rows | 20100505_4a455987-e6bf-4794-89ba-147d5d4834b2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 50653-3001-1 | 50653300101 | 100 mL in 1 BOTTLE, WITH APPLICATOR | 100 ml | Historical |
| 50653-3001-2 | 50653300102 | 150 mL in 1 BOTTLE, WITH APPLICATOR | 150 ml | Historical |