Product NDC: | 49404-106 |
Proprietary Name: | Dr.Jart Renewalist BB |
Non Proprietary Name: | Titanium Dioxide, Zinc Oxide |
Active Ingredient(s): | 2.704; 1.891 mL/30mL; mL/30mL & nbsp; Titanium Dioxide, Zinc Oxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49404-106 |
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: | 20120730 |
Package NDC: | 49404-106-02 |
Package Description: | 1 TUBE in 1 CARTON (49404-106-02) > 40 mL in 1 TUBE (49404-106-01) |
NDC Code | 49404-106-02 |
Proprietary Name | Dr.Jart Renewalist BB |
Package Description | 1 TUBE in 1 CARTON (49404-106-02) > 40 mL in 1 TUBE (49404-106-01) |
Product NDC | 49404-106 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Titanium Dioxide, Zinc Oxide |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120730 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Have and Be Co., Ltd. |
Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 2.704; 1.891 |
Strength Unit | mL/30mL; mL/30mL |
Pharmaceutical Classes |