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Lancome - 49967-839-01 - (Octinoxate)
Drug Information of Lancome
| Product NDC: | 49967-839 |
| Proprietary Name: | Lancome |
| Non Proprietary Name: | Octinoxate |
| Active Ingredient(s): | .9 mL/30mL & nbsp; Octinoxate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lancome
| Product NDC: | 49967-839 |
| Labeler Name: | L'Oreal USA Products Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111101 |
Package Information of Lancome
| Package NDC: | 49967-839-01 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (49967-839-01) > 30 mL in 1 BOTTLE, PUMP |
NDC Information of Lancome
| NDC Code | 49967-839-01 |
| Proprietary Name | Lancome |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (49967-839-01) > 30 mL in 1 BOTTLE, PUMP |
| Product NDC | 49967-839 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20111101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | L'Oreal USA Products Inc |
| Substance Name | OCTINOXATE |
| Strength Number | .9 |
| Strength Unit | mL/30mL |
| Pharmaceutical Classes |
