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Pure Finish Mineral Tinted Moisturizer SPF 15
Pure Finish Mineral Tinted Moisturizer SPF 15 - 67938-110-01 - (Octinoxate)
Drug Information of Pure Finish Mineral Tinted Moisturizer SPF 15
| Product NDC: | 67938-110 |
| Proprietary Name: | Pure Finish Mineral Tinted Moisturizer SPF 15 |
| Non Proprietary Name: | Octinoxate |
| Active Ingredient(s): | 3; 2; 2.15 mL/50mL; mL/50mL; mL/50mL & nbsp; Octinoxate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pure Finish Mineral Tinted Moisturizer SPF 15
| Product NDC: | 67938-110 |
| Labeler Name: | Elizabeth Arden, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100726 |
Package Information of Pure Finish Mineral Tinted Moisturizer SPF 15
| Package NDC: | 67938-110-01 |
| Package Description: | 1 TUBE in 1 BOX (67938-110-01) > 50 mL in 1 TUBE (67938-110-02) |
NDC Information of Pure Finish Mineral Tinted Moisturizer SPF 15
| NDC Code | 67938-110-01 |
| Proprietary Name | Pure Finish Mineral Tinted Moisturizer SPF 15 |
| Package Description | 1 TUBE in 1 BOX (67938-110-01) > 50 mL in 1 TUBE (67938-110-02) |
| Product NDC | 67938-110 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100726 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Elizabeth Arden, Inc |
| Substance Name | OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE |
| Strength Number | 3; 2; 2.15 |
| Strength Unit | mL/50mL; mL/50mL; mL/50mL |
| Pharmaceutical Classes |
