| Product NDC: | 67938-0801 |
| Proprietary Name: | Elizabeth Arden Moisture Shield SPF 15 |
| Non Proprietary Name: | Octinoxate |
| Active Ingredient(s): | .75; 3.125; 2.5; 1 mL/50mL; mL/50mL; mL/50mL; mL/50mL & nbsp; Octinoxate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 67938-0801 |
| Labeler Name: | Elizabeth Arden, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20060626 |
| Package NDC: | 67938-0801-1 |
| Package Description: | 1 BOTTLE, PUMP in 1 BOX (67938-0801-1) > 50 mL in 1 BOTTLE, PUMP (67938-0801-2) |
| NDC Code | 67938-0801-1 |
| Proprietary Name | Elizabeth Arden Moisture Shield SPF 15 |
| Package Description | 1 BOTTLE, PUMP in 1 BOX (67938-0801-1) > 50 mL in 1 BOTTLE, PUMP (67938-0801-2) |
| Product NDC | 67938-0801 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20060626 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Elizabeth Arden, Inc |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | .75; 3.125; 2.5; 1 |
| Strength Unit | mL/50mL; mL/50mL; mL/50mL; mL/50mL |
| Pharmaceutical Classes |