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Pure Finish Mineral Powder Foundation SPF 20 Pure Finish 7
Pure Finish Mineral Powder Foundation SPF 20 Pure Finish 7 - 67938-1396-1 - (Titanium Dioxide)
Drug Information of Pure Finish Mineral Powder Foundation SPF 20 Pure Finish 7
| Product NDC: | 67938-1396 |
| Proprietary Name: | Pure Finish Mineral Powder Foundation SPF 20 Pure Finish 7 |
| Non Proprietary Name: | Titanium Dioxide |
| Active Ingredient(s): | .358 g/8.33g & nbsp; Titanium Dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pure Finish Mineral Powder Foundation SPF 20 Pure Finish 7
| Product NDC: | 67938-1396 |
| Labeler Name: | Elizabeth Arden, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100920 |
Package Information of Pure Finish Mineral Powder Foundation SPF 20 Pure Finish 7
| Package NDC: | 67938-1396-1 |
| Package Description: | 1 CONTAINER in 1 BOX (67938-1396-1) > 8.33 g in 1 CONTAINER (67938-1396-2) |
NDC Information of Pure Finish Mineral Powder Foundation SPF 20 Pure Finish 7
| NDC Code | 67938-1396-1 |
| Proprietary Name | Pure Finish Mineral Powder Foundation SPF 20 Pure Finish 7 |
| Package Description | 1 CONTAINER in 1 BOX (67938-1396-1) > 8.33 g in 1 CONTAINER (67938-1396-2) |
| Product NDC | 67938-1396 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium Dioxide |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20100920 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Elizabeth Arden, Inc |
| Substance Name | TITANIUM DIOXIDE |
| Strength Number | .358 |
| Strength Unit | g/8.33g |
| Pharmaceutical Classes |
