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Divine Illumination Divine Flawless Foundation
Divine Illumination Divine Flawless Foundation - 50184-7000-1 - (TITANIUM DIOXIDE AND ZINC OXIDE)
Drug Information of Divine Illumination Divine Flawless Foundation
| Product NDC: | 50184-7000 |
| Proprietary Name: | Divine Illumination Divine Flawless Foundation |
| Non Proprietary Name: | TITANIUM DIOXIDE AND ZINC OXIDE |
| Active Ingredient(s): | 4.68; 4.5 mL/45mL; mL/45mL & nbsp; TITANIUM DIOXIDE AND ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Divine Illumination Divine Flawless Foundation
| Product NDC: | 50184-7000 |
| Labeler Name: | Philosophy, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120114 |
Package Information of Divine Illumination Divine Flawless Foundation
| Package NDC: | 50184-7000-1 |
| Package Description: | 45 mL in 1 TUBE (50184-7000-1) |
NDC Information of Divine Illumination Divine Flawless Foundation
| NDC Code | 50184-7000-1 |
| Proprietary Name | Divine Illumination Divine Flawless Foundation |
| Package Description | 45 mL in 1 TUBE (50184-7000-1) |
| Product NDC | 50184-7000 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE AND ZINC OXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120114 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Philosophy, Inc. |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 4.68; 4.5 |
| Strength Unit | mL/45mL; mL/45mL |
| Pharmaceutical Classes |
