Home
>
National Drug Code (NDC)
>
LOreal Paris Dermo Expertise
LOreal Paris Dermo Expertise - 49967-159-01 - (Ensulizole Octinoxate)
Drug Information of LOreal Paris Dermo Expertise
| Product NDC: | 49967-159 |
| Proprietary Name: | LOreal Paris Dermo Expertise |
| Non Proprietary Name: | Ensulizole Octinoxate |
| Active Ingredient(s): | 2.36; 8.26 mL/118mL; mL/118mL & nbsp; Ensulizole Octinoxate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LOreal Paris Dermo Expertise
| Product NDC: | 49967-159 |
| 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: | 20110701 |
Package Information of LOreal Paris Dermo Expertise
| Package NDC: | 49967-159-01 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (49967-159-01) > 118 mL in 1 BOTTLE, PLASTIC |
NDC Information of LOreal Paris Dermo Expertise
| NDC Code | 49967-159-01 |
| Proprietary Name | LOreal Paris Dermo Expertise |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (49967-159-01) > 118 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 49967-159 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ensulizole Octinoxate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110701 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | L'Oreal USA Products Inc |
| Substance Name | ENSULIZOLE; OCTINOXATE |
| Strength Number | 2.36; 8.26 |
| Strength Unit | mL/118mL; mL/118mL |
| Pharmaceutical Classes |
