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Rendrevie Sun Screen SPF35 PA
Rendrevie Sun Screen SPF35 PA - 76173-1001-2 - (OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE)
Drug Information of Rendrevie Sun Screen SPF35 PA
| Product NDC: | 76173-1001 |
| Proprietary Name: | Rendrevie Sun Screen SPF35 PA |
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE |
| Active Ingredient(s): | 5.625; 2.25; 3.89 mL/75mL; mL/75mL; mL/75mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Rendrevie Sun Screen SPF35 PA
| Product NDC: | 76173-1001 |
| Labeler Name: | Cellinbio Co Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110720 |
Package Information of Rendrevie Sun Screen SPF35 PA
| Package NDC: | 76173-1001-2 |
| Package Description: | 1 TUBE in 1 BOX (76173-1001-2) > 75 mL in 1 TUBE (76173-1001-1) |
NDC Information of Rendrevie Sun Screen SPF35 PA
| NDC Code | 76173-1001-2 |
| Proprietary Name | Rendrevie Sun Screen SPF35 PA |
| Package Description | 1 TUBE in 1 BOX (76173-1001-2) > 75 mL in 1 TUBE (76173-1001-1) |
| Product NDC | 76173-1001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110720 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Cellinbio Co Ltd |
| Substance Name | OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE |
| Strength Number | 5.625; 2.25; 3.89 |
| Strength Unit | mL/75mL; mL/75mL; mL/75mL |
| Pharmaceutical Classes |
