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shu uemura UV underbase
shu uemura UV underbase - 68570-704-01 - (Octinoxate Titanium Dioxide)
Drug Information of shu uemura UV underbase
| Product NDC: | 68570-704 |
| Proprietary Name: | shu uemura UV underbase |
| Non Proprietary Name: | Octinoxate Titanium Dioxide |
| Active Ingredient(s): | .84; 1.428 mL/28mL; mL/28mL & nbsp; Octinoxate Titanium Dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of shu uemura UV underbase
| Product NDC: | 68570-704 |
| Labeler Name: | Cosmelor Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20091001 |
Package Information of shu uemura UV underbase
| Package NDC: | 68570-704-01 |
| Package Description: | 1 TUBE in 1 CARTON (68570-704-01) > 28 mL in 1 TUBE |
NDC Information of shu uemura UV underbase
| NDC Code | 68570-704-01 |
| Proprietary Name | shu uemura UV underbase |
| Package Description | 1 TUBE in 1 CARTON (68570-704-01) > 28 mL in 1 TUBE |
| Product NDC | 68570-704 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate Titanium Dioxide |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20091001 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Cosmelor Ltd |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | .84; 1.428 |
| Strength Unit | mL/28mL; mL/28mL |
| Pharmaceutical Classes |
