 
                        | Product NDC: | 10096-0103 | 
| Proprietary Name: | moisture therapy | 
| Non Proprietary Name: | Octinoxate, Oxybenzone | 
| Active Ingredient(s): | 1.125; .45 mL/15mL; mL/15mL & nbsp; Octinoxate, Oxybenzone | 
| Administration Route(s): | TOPICAL | 
| Dosage Form(s): | OINTMENT | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 10096-0103 | 
| Labeler Name: | Avon Products, Inc. | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part352 | 
| Marketing Category: | OTC MONOGRAPH NOT FINAL | 
| Start Marketing Date: | 20120522 | 
| Package NDC: | 10096-0103-1 | 
| Package Description: | 15 mL in 1 TUBE, WITH APPLICATOR (10096-0103-1) | 
| NDC Code | 10096-0103-1 | 
| Proprietary Name | moisture therapy | 
| Package Description | 15 mL in 1 TUBE, WITH APPLICATOR (10096-0103-1) | 
| Product NDC | 10096-0103 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Octinoxate, Oxybenzone | 
| Dosage Form Name | OINTMENT | 
| Route Name | TOPICAL | 
| Start Marketing Date | 20120522 | 
| Marketing Category Name | OTC MONOGRAPH NOT FINAL | 
| Labeler Name | Avon Products, Inc. | 
| Substance Name | OCTINOXATE; OXYBENZONE | 
| Strength Number | 1.125; .45 | 
| Strength Unit | mL/15mL; mL/15mL | 
| Pharmaceutical Classes |