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Dolce and Gabbana Perfect Luminous Foundation
Dolce and Gabbana Perfect Luminous Foundation - 37000-398-30 - (Octinoxate and Titanium Dioxide)
Drug Information of Dolce and Gabbana Perfect Luminous Foundation
| Product NDC: | 37000-398 |
| Proprietary Name: | Dolce and Gabbana Perfect Luminous Foundation |
| Non Proprietary Name: | Octinoxate and Titanium Dioxide |
| Active Ingredient(s): | 40; 40 mg/mL; mg/mL & nbsp; Octinoxate and Titanium Dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dolce and Gabbana Perfect Luminous Foundation
| Product NDC: | 37000-398 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130121 |
Package Information of Dolce and Gabbana Perfect Luminous Foundation
| Package NDC: | 37000-398-30 |
| Package Description: | 1 JAR in 1 CARTON (37000-398-30) > 30 mL in 1 JAR |
NDC Information of Dolce and Gabbana Perfect Luminous Foundation
| NDC Code | 37000-398-30 |
| Proprietary Name | Dolce and Gabbana Perfect Luminous Foundation |
| Package Description | 1 JAR in 1 CARTON (37000-398-30) > 30 mL in 1 JAR |
| Product NDC | 37000-398 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate and Titanium Dioxide |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20130121 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Procter & Gamble Manufacturing Company |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 40; 40 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
