| Product NDC: | 75949-4001 |
| Proprietary Name: | ELCURE AC-LEX Serum |
| Non Proprietary Name: | AZELAIC ACID |
| Active Ingredient(s): | 2.5 mL/50mL & nbsp; AZELAIC ACID |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 75949-4001 |
| Labeler Name: | Elcure Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20111124 |
| Package NDC: | 75949-4001-1 |
| Package Description: | 50 mL in 1 BOTTLE, GLASS (75949-4001-1) |
| NDC Code | 75949-4001-1 |
| Proprietary Name | ELCURE AC-LEX Serum |
| Package Description | 50 mL in 1 BOTTLE, GLASS (75949-4001-1) |
| Product NDC | 75949-4001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AZELAIC ACID |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20111124 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Elcure Co., Ltd. |
| Substance Name | AZELAIC ACID |
| Strength Number | 2.5 |
| Strength Unit | mL/50mL |
| Pharmaceutical Classes |