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Dr.eslee Sun Matte
Dr.eslee Sun Matte - 76340-3001-1 - (OCTINOXATE)
Drug Information of Dr.eslee Sun Matte
| Product NDC: | 76340-3001 |
| Proprietary Name: | Dr.eslee Sun Matte |
| Non Proprietary Name: | OCTINOXATE |
| Active Ingredient(s): | 7.5 g/100g & nbsp; OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dr.eslee Sun Matte
| Product NDC: | 76340-3001 |
| Labeler Name: | Ajou Medics Co., Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110810 |
Package Information of Dr.eslee Sun Matte
| Package NDC: | 76340-3001-1 |
| Package Description: | 60 g in 1 TUBE (76340-3001-1) |
NDC Information of Dr.eslee Sun Matte
| NDC Code | 76340-3001-1 |
| Proprietary Name | Dr.eslee Sun Matte |
| Package Description | 60 g in 1 TUBE (76340-3001-1) |
| Product NDC | 76340-3001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20110810 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Ajou Medics Co., Ltd |
| Substance Name | OCTINOXATE |
| Strength Number | 7.5 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
