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ARTISTRY Time Defiance UV Defense SPF 50 Ultra Facial Sunscreen
ARTISTRY Time Defiance UV Defense SPF 50 Ultra Facial Sunscreen - 50390-110-30 - (OCTINOXATE, ZINC OXIDE, OCTISALATE,TITANIUM DIOXIDE)
Drug Information of ARTISTRY Time Defiance UV Defense SPF 50 Ultra Facial Sunscreen
| Product NDC: | 50390-110 |
| Proprietary Name: | ARTISTRY Time Defiance UV Defense SPF 50 Ultra Facial Sunscreen |
| Non Proprietary Name: | OCTINOXATE, ZINC OXIDE, OCTISALATE,TITANIUM DIOXIDE |
| Active Ingredient(s): | 7.5; 5; 2.49; 6.528 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, ZINC OXIDE, OCTISALATE,TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ARTISTRY Time Defiance UV Defense SPF 50 Ultra Facial Sunscreen
| Product NDC: | 50390-110 |
| Labeler Name: | Amway Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120510 |
Package Information of ARTISTRY Time Defiance UV Defense SPF 50 Ultra Facial Sunscreen
| Package NDC: | 50390-110-30 |
| Package Description: | 30 mL in 1 BOTTLE (50390-110-30) |
NDC Information of ARTISTRY Time Defiance UV Defense SPF 50 Ultra Facial Sunscreen
| NDC Code | 50390-110-30 |
| Proprietary Name | ARTISTRY Time Defiance UV Defense SPF 50 Ultra Facial Sunscreen |
| Package Description | 30 mL in 1 BOTTLE (50390-110-30) |
| Product NDC | 50390-110 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, ZINC OXIDE, OCTISALATE,TITANIUM DIOXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120510 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Amway Corp |
| Substance Name | OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 7.5; 5; 2.49; 6.528 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
