| Product NDC: | 49817-0062 |
| Proprietary Name: | GUERLAIN LINGERIE DE PEAU INVISIBLE SKIN-FUSION FOUNDATION WITH SUNSCREEN BROAD SPECTRUM SPF 20 31 AMBRE PALE |
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE |
| Active Ingredient(s): | 3; 3.16 mL/100mL; mL/100mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49817-0062 |
| Labeler Name: | Guerlain S.A |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120727 |
| Package NDC: | 49817-0062-1 |
| Package Description: | 1 BOTTLE in 1 CARTON (49817-0062-1) > 30 mL in 1 BOTTLE |
| NDC Code | 49817-0062-1 |
| Proprietary Name | GUERLAIN LINGERIE DE PEAU INVISIBLE SKIN-FUSION FOUNDATION WITH SUNSCREEN BROAD SPECTRUM SPF 20 31 AMBRE PALE |
| Package Description | 1 BOTTLE in 1 CARTON (49817-0062-1) > 30 mL in 1 BOTTLE |
| Product NDC | 49817-0062 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120727 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Guerlain S.A |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 3; 3.16 |
| Strength Unit | mL/100mL; mL/100mL |
| Pharmaceutical Classes |