| Product NDC: | 49404-107 |
| Proprietary Name: | Dr.Jart Black Label Detox BB Beaty Balm |
| Non Proprietary Name: | Titanium Dioxide, Zinc Oxide |
| Active Ingredient(s): | 3.8132; 1.536 mL/40mL; mL/40mL & nbsp; Titanium Dioxide, Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49404-107 |
| Labeler Name: | Have and Be Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120901 |
| Package NDC: | 49404-107-02 |
| Package Description: | 1 TUBE in 1 CARTON (49404-107-02) > 40 mL in 1 TUBE (49404-107-01) |
| NDC Code | 49404-107-02 |
| Proprietary Name | Dr.Jart Black Label Detox BB Beaty Balm |
| Package Description | 1 TUBE in 1 CARTON (49404-107-02) > 40 mL in 1 TUBE (49404-107-01) |
| Product NDC | 49404-107 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium Dioxide, Zinc Oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Have and Be Co., Ltd. |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 3.8132; 1.536 |
| Strength Unit | mL/40mL; mL/40mL |
| Pharmaceutical Classes |