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NouriFusion
NouriFusion - 51785-515-01 - (Avobenzone, Octinoxate, Octisalate)
Drug Information of NouriFusion
| Product NDC: | 51785-515 |
| Proprietary Name: | NouriFusion |
| Non Proprietary Name: | Avobenzone, Octinoxate, Octisalate |
| Active Ingredient(s): | 1.079; 3.535; 1.52 g/50mL; g/50mL; g/50mL & nbsp; Avobenzone, Octinoxate, Octisalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NouriFusion
| Product NDC: | 51785-515 |
| Labeler Name: | Herbalife International of America Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120925 |
Package Information of NouriFusion
| Package NDC: | 51785-515-01 |
| Package Description: | 50 mL in 1 TUBE (51785-515-01) |
NDC Information of NouriFusion
| NDC Code | 51785-515-01 |
| Proprietary Name | NouriFusion |
| Package Description | 50 mL in 1 TUBE (51785-515-01) |
| Product NDC | 51785-515 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octinoxate, Octisalate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120925 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Herbalife International of America Inc. |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE |
| Strength Number | 1.079; 3.535; 1.52 |
| Strength Unit | g/50mL; g/50mL; g/50mL |
| Pharmaceutical Classes |
