| Product NDC: | 58414-2047 |
| Proprietary Name: | Exuviance Sheer Refining Fluid SPF 35 |
| Non Proprietary Name: | OCTINOXATE, OCTISALATE, and AVOBENZONE |
| Active Ingredient(s): | 30; 75; 50 mg/mL; mg/mL; mg/mL & nbsp; OCTINOXATE, OCTISALATE, and AVOBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 58414-2047 |
| Labeler Name: | NeoStrata Company Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130702 |
| Package NDC: | 58414-2047-1 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (58414-2047-1) > 50 mL in 1 BOTTLE, PUMP |
| NDC Code | 58414-2047-1 |
| Proprietary Name | Exuviance Sheer Refining Fluid SPF 35 |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (58414-2047-1) > 50 mL in 1 BOTTLE, PUMP |
| Product NDC | 58414-2047 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTISALATE, and AVOBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130702 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | NeoStrata Company Inc. |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE |
| Strength Number | 30; 75; 50 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |