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La Prairie
La Prairie - 76157-301-13 - (Avobenzone, Octinoxate, Octisalate)
Drug Information of La Prairie
| Product NDC: | 76157-301 |
| Proprietary Name: | La Prairie |
| Non Proprietary Name: | Avobenzone, Octinoxate, Octisalate |
| Active Ingredient(s): | 3; 7.5; 5 kg/100kg; kg/100kg; kg/100kg & nbsp; Avobenzone, Octinoxate, Octisalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of La Prairie
| Product NDC: | 76157-301 |
| Labeler Name: | La Prairie Group AG |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090101 |
Package Information of La Prairie
| Package NDC: | 76157-301-13 |
| Package Description: | 1 BOTTLE in 1 BOX (76157-301-13) > .05 kg in 1 BOTTLE (76157-301-12) |
NDC Information of La Prairie
| NDC Code | 76157-301-13 |
| Proprietary Name | La Prairie |
| Package Description | 1 BOTTLE in 1 BOX (76157-301-13) > .05 kg in 1 BOTTLE (76157-301-12) |
| Product NDC | 76157-301 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octinoxate, Octisalate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20090101 |
| 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 | kg/100kg; kg/100kg; kg/100kg |
| Pharmaceutical Classes |
