Product NDC: | 10096-0173 |
Proprietary Name: | mark. get a tint |
Non Proprietary Name: | Octinoxate, Titanium Dioxide |
Active Ingredient(s): | 2.995; 2.905 mL/50mL; mL/50mL & nbsp; Octinoxate, Titanium Dioxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10096-0173 |
Labeler Name: | Avon Products, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120523 |
Package NDC: | 10096-0173-2 |
Package Description: | 1 TUBE in 1 CARTON (10096-0173-2) > 50 mL in 1 TUBE (10096-0173-1) |
NDC Code | 10096-0173-2 |
Proprietary Name | mark. get a tint |
Package Description | 1 TUBE in 1 CARTON (10096-0173-2) > 50 mL in 1 TUBE (10096-0173-1) |
Product NDC | 10096-0173 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate, Titanium Dioxide |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20120523 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Avon Products, Inc. |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
Strength Number | 2.995; 2.905 |
Strength Unit | mL/50mL; mL/50mL |
Pharmaceutical Classes |