| Product NDC: | 49404-115 |
| Proprietary Name: | Dr.Jart CC Essence Balm 02 Medium - Deep |
| Non Proprietary Name: | Titanium Dioxide, OCTINOXATE, Zinc Oxide, OCTISALATE |
| Active Ingredient(s): | .48; .192; 1.147; .279 g/12g; g/12g; g/12g; g/12g & nbsp; Titanium Dioxide, OCTINOXATE, Zinc Oxide, OCTISALATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49404-115 |
| 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: | 20130415 |
| Package NDC: | 49404-115-02 |
| Package Description: | 1 JAR in 1 CARTON (49404-115-02) > 12 g in 1 JAR (49404-115-01) |
| NDC Code | 49404-115-02 |
| Proprietary Name | Dr.Jart CC Essence Balm 02 Medium - Deep |
| Package Description | 1 JAR in 1 CARTON (49404-115-02) > 12 g in 1 JAR (49404-115-01) |
| Product NDC | 49404-115 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium Dioxide, OCTINOXATE, Zinc Oxide, OCTISALATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130415 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Have and Be Co., Ltd. |
| Substance Name | OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | .48; .192; 1.147; .279 |
| Strength Unit | g/12g; g/12g; g/12g; g/12g |
| Pharmaceutical Classes |