| Product NDC: | 10096-0185 | 
| Proprietary Name: | Clearskin Professional | 
| Non Proprietary Name: | OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE | 
| Active Ingredient(s): | 25; 71.1; 45; 30 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE | 
| Administration Route(s): | TOPICAL | 
| Dosage Form(s): | LOTION | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 10096-0185 | 
| Labeler Name: | Avon Products, Inc. | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part352 | 
| Marketing Category: | OTC MONOGRAPH NOT FINAL | 
| Start Marketing Date: | 20091221 | 
| Package NDC: | 10096-0185-2 | 
| Package Description: | 1 TUBE in 1 CARTON (10096-0185-2) > 75 mL in 1 TUBE (10096-0185-1) | 
| NDC Code | 10096-0185-2 | 
| Proprietary Name | Clearskin Professional | 
| Package Description | 1 TUBE in 1 CARTON (10096-0185-2) > 75 mL in 1 TUBE (10096-0185-1) | 
| Product NDC | 10096-0185 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE | 
| Dosage Form Name | LOTION | 
| Route Name | TOPICAL | 
| Start Marketing Date | 20091221 | 
| Marketing Category Name | OTC MONOGRAPH NOT FINAL | 
| Labeler Name | Avon Products, Inc. | 
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE | 
| Strength Number | 25; 71.1; 45; 30 | 
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL | 
| Pharmaceutical Classes |