Home
>
National Drug Code (NDC)
>
La Praire Switzerland
La Praire Switzerland - 76157-321-02 - (Avobenzone, Octinoxate, Octisalate)
Drug Information of La Praire Switzerland
| Product NDC: | 76157-321 |
| Proprietary Name: | La Praire Switzerland |
| Non Proprietary Name: | Avobenzone, Octinoxate, Octisalate |
| Active Ingredient(s): | 3; 7.5; 5 mL/50mL; mL/50mL; mL/50mL & nbsp; Avobenzone, Octinoxate, Octisalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of La Praire Switzerland
| Product NDC: | 76157-321 |
| Labeler Name: | La Prairie Group AG |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110617 |
Package Information of La Praire Switzerland
| Package NDC: | 76157-321-02 |
| Package Description: | 1 BOTTLE in 1 BOX (76157-321-02) > 50 mL in 1 BOTTLE (76157-321-01) |
NDC Information of La Praire Switzerland
| NDC Code | 76157-321-02 |
| Proprietary Name | La Praire Switzerland |
| Package Description | 1 BOTTLE in 1 BOX (76157-321-02) > 50 mL in 1 BOTTLE (76157-321-01) |
| Product NDC | 76157-321 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octinoxate, Octisalate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110617 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | La Prairie Group AG |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE |
| Strength Number | 3; 7.5; 5 |
| Strength Unit | mL/50mL; mL/50mL; mL/50mL |
| Pharmaceutical Classes |
