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Bonogen
Bonogen - 50653-1001-1 - (panthenol)
Drug Information of Bonogen
| Product NDC: | 50653-1001 |
| Proprietary Name: | Bonogen |
| Non Proprietary Name: | panthenol |
| Active Ingredient(s): | .06; .3; .5; 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) |
Labeler Information of Bonogen
| Product NDC: | 50653-1001 |
| Labeler Name: | Bonogen Co., Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100301 |
Package Information of Bonogen
| Package NDC: | 50653-1001-1 |
| Package Description: | 100 g in 1 BOTTLE (50653-1001-1) |
NDC Information of Bonogen
| NDC Code | 50653-1001-1 |
| Proprietary Name | Bonogen |
| Package Description | 100 g in 1 BOTTLE (50653-1001-1) |
| Product NDC | 50653-1001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | panthenol |
| Dosage Form Name | SHAMPOO |
| Route Name | TOPICAL |
| Start Marketing Date | 20100301 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Bonogen Co., Ltd |
| Substance Name | BIOTIN; NADIDE; PANTHENOL; PYRITHIONE ZINC |
| Strength Number | .06; .3; .5; 2.1 |
| Strength Unit | g/100g; g/100g; g/100g; g/100g |
| Pharmaceutical Classes |
