| 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 |