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) |
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 NDC: | 76173-1001-2 |
Package Description: | 1 TUBE in 1 BOX (76173-1001-2) > 75 mL in 1 TUBE (76173-1001-1) |
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 |