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Yves Saint Laurent
Yves Saint Laurent - 49967-521-01 - (Octinoxate)
Drug Information of Yves Saint Laurent
| Product NDC: | 49967-521 |
| Proprietary Name: | Yves Saint Laurent |
| Non Proprietary Name: | Octinoxate |
| Active Ingredient(s): | .6 g/10g & nbsp; Octinoxate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Yves Saint Laurent
| Product NDC: | 49967-521 |
| 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: | 20110801 |
Package Information of Yves Saint Laurent
| Package NDC: | 49967-521-01 |
| Package Description: | 1 CASE in 1 CARTON (49967-521-01) > 10 g in 1 CASE |
NDC Information of Yves Saint Laurent
| NDC Code | 49967-521-01 |
| Proprietary Name | Yves Saint Laurent |
| Package Description | 1 CASE in 1 CARTON (49967-521-01) > 10 g in 1 CASE |
| Product NDC | 49967-521 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20110801 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | L'Oreal USA Products Inc |
| Substance Name | OCTINOXATE |
| Strength Number | .6 |
| Strength Unit | g/10g |
| Pharmaceutical Classes |
