Product NDC: | 10096-0231 |
Proprietary Name: | Extralasting |
Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE |
Active Ingredient(s): | 63.4; 30 mg/g; mg/g & nbsp; OCTINOXATE, TITANIUM DIOXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10096-0231 |
Labeler Name: | Avon Products, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20101215 |
Package NDC: | 10096-0231-2 |
Package Description: | 1 CASE in 1 CARTON (10096-0231-2) > 9 g in 1 CASE (10096-0231-1) |
NDC Code | 10096-0231-2 |
Proprietary Name | Extralasting |
Package Description | 1 CASE in 1 CARTON (10096-0231-2) > 9 g in 1 CASE (10096-0231-1) |
Product NDC | 10096-0231 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20101215 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Avon Products, Inc. |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
Strength Number | 63.4; 30 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes |