Product NDC: | 59351-0314 |
Proprietary Name: | Rimmel London |
Non Proprietary Name: | Octinoxate, Octisalate |
Active Ingredient(s): | .012; .12 mL/6mL; mL/6mL & nbsp; Octinoxate, Octisalate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59351-0314 |
Labeler Name: | Lancaster S.A.M. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20101020 |
Package NDC: | 59351-0314-1 |
Package Description: | 6 mL in 1 TUBE (59351-0314-1) |
NDC Code | 59351-0314-1 |
Proprietary Name | Rimmel London |
Package Description | 6 mL in 1 TUBE (59351-0314-1) |
Product NDC | 59351-0314 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate, Octisalate |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20101020 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Lancaster S.A.M. |
Substance Name | OCTINOXATE; OCTISALATE |
Strength Number | .012; .12 |
Strength Unit | mL/6mL; mL/6mL |
Pharmaceutical Classes |