Product NDC: | 50653-2001 |
Proprietary Name: | Bonogen Plus |
Non Proprietary Name: | panthenol |
Active Ingredient(s): | .06; .3; .6; 2.1 g/100g; g/100g; g/100g; g/100g & nbsp; panthenol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SHAMPOO |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50653-2001 |
Labeler Name: | Bonogen Co., Ltd |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20100409 |
Package NDC: | 50653-2001-1 |
Package Description: | 100 g in 1 BOTTLE (50653-2001-1) |
NDC Code | 50653-2001-1 |
Proprietary Name | Bonogen Plus |
Package Description | 100 g in 1 BOTTLE (50653-2001-1) |
Product NDC | 50653-2001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | panthenol |
Dosage Form Name | SHAMPOO |
Route Name | TOPICAL |
Start Marketing Date | 20100409 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Bonogen Co., Ltd |
Substance Name | BIOTIN; NADIDE; PANTHENOL; PYRITHIONE ZINC |
Strength Number | .06; .3; .6; 2.1 |
Strength Unit | g/100g; g/100g; g/100g; g/100g |
Pharmaceutical Classes |