Product NDC: | 59351-0318 |
Proprietary Name: | Rimmel London |
Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE |
Active Ingredient(s): | 1.2; .9 mL/30mL; mL/30mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59351-0318 |
Labeler Name: | Lancaster S.A.M. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20101006 |
Package NDC: | 59351-0318-1 |
Package Description: | 30 mL in 1 BOTTLE, DISPENSING (59351-0318-1) |
NDC Code | 59351-0318-1 |
Proprietary Name | Rimmel London |
Package Description | 30 mL in 1 BOTTLE, DISPENSING (59351-0318-1) |
Product NDC | 59351-0318 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20101006 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Lancaster S.A.M. |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
Strength Number | 1.2; .9 |
Strength Unit | mL/30mL; mL/30mL |
Pharmaceutical Classes |