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Fresh Umbrian Clay Freshface Foundation SPF 20 Sun Empress
Fresh Umbrian Clay Freshface Foundation SPF 20 Sun Empress - 49817-1991-5 - (Octinoxate)
Drug Information of Fresh Umbrian Clay Freshface Foundation SPF 20 Sun Empress
| Product NDC: | 49817-1991 |
| Proprietary Name: | Fresh Umbrian Clay Freshface Foundation SPF 20 Sun Empress |
| Non Proprietary Name: | Octinoxate |
| Active Ingredient(s): | 3 g/100g & nbsp; Octinoxate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fresh Umbrian Clay Freshface Foundation SPF 20 Sun Empress
| Product NDC: | 49817-1991 |
| Labeler Name: | Guerlain |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090401 |
Package Information of Fresh Umbrian Clay Freshface Foundation SPF 20 Sun Empress
| Package NDC: | 49817-1991-5 |
| Package Description: | 1 BOTTLE in 1 CARTON (49817-1991-5) > 33 g in 1 BOTTLE (49817-1991-9) |
NDC Information of Fresh Umbrian Clay Freshface Foundation SPF 20 Sun Empress
| NDC Code | 49817-1991-5 |
| Proprietary Name | Fresh Umbrian Clay Freshface Foundation SPF 20 Sun Empress |
| Package Description | 1 BOTTLE in 1 CARTON (49817-1991-5) > 33 g in 1 BOTTLE (49817-1991-9) |
| Product NDC | 49817-1991 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate |
| Dosage Form Name | EMULSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20090401 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Guerlain |
| Substance Name | OCTINOXATE |
| Strength Number | 3 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
