| Product NDC: | 43948-1101 |
| Proprietary Name: | Dr. Young 2P Pearl Brightening Balm SPF35 PA |
| Non Proprietary Name: | ALLANTOIN |
| Active Ingredient(s): | .5 mg/100mL & nbsp; ALLANTOIN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 43948-1101 |
| Labeler Name: | The Doctors Cosmetics Co., Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120927 |
| Package NDC: | 43948-1101-1 |
| Package Description: | 30 mL in 1 TUBE (43948-1101-1) |
| NDC Code | 43948-1101-1 |
| Proprietary Name | Dr. Young 2P Pearl Brightening Balm SPF35 PA |
| Package Description | 30 mL in 1 TUBE (43948-1101-1) |
| Product NDC | 43948-1101 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALLANTOIN |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120927 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | The Doctors Cosmetics Co., Ltd |
| Substance Name | ALLANTOIN |
| Strength Number | .5 |
| Strength Unit | mg/100mL |
| Pharmaceutical Classes |