| 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 |