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AGE-X Platinum BB
AGE-X Platinum BB - 49404-104-02 - (Titanium Dioxide, Octinoxate)
Drug Information of AGE-X Platinum BB
| Product NDC: | 49404-104 |
| Proprietary Name: | AGE-X Platinum BB |
| Non Proprietary Name: | Titanium Dioxide, Octinoxate |
| Active Ingredient(s): | 2.1; 1.68 mL/30mL; mL/30mL & nbsp; Titanium Dioxide, Octinoxate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AGE-X Platinum BB
| Product NDC: | 49404-104 |
| 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: | 20101201 |
Package Information of AGE-X Platinum BB
| Package NDC: | 49404-104-02 |
| Package Description: | 1 TUBE in 1 CARTON (49404-104-02) > 30 mL in 1 TUBE (49404-104-01) |
NDC Information of AGE-X Platinum BB
| NDC Code | 49404-104-02 |
| Proprietary Name | AGE-X Platinum BB |
| Package Description | 1 TUBE in 1 CARTON (49404-104-02) > 30 mL in 1 TUBE (49404-104-01) |
| Product NDC | 49404-104 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium Dioxide, Octinoxate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20101201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Have and Be Co., Ltd. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 2.1; 1.68 |
| Strength Unit | mL/30mL; mL/30mL |
| Pharmaceutical Classes |
