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Elta MD UV SPF46
Elta MD UV SPF46 - 60232-2585-4 - (zinc oxide and octinoxate sunscreen)
Drug Information of Elta MD UV SPF46
| Product NDC: | 60232-2585 |
| Proprietary Name: | Elta MD UV SPF46 |
| Non Proprietary Name: | zinc oxide and octinoxate sunscreen |
| Active Ingredient(s): | 75; 93 g/1000g; g/1000g & nbsp; zinc oxide and octinoxate sunscreen |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Elta MD UV SPF46
| Product NDC: | 60232-2585 |
| Labeler Name: | Swiss American Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100601 |
Package Information of Elta MD UV SPF46
| Package NDC: | 60232-2585-4 |
| Package Description: | 4 g in 1 BOTTLE, SPRAY (60232-2585-4) |
NDC Information of Elta MD UV SPF46
| NDC Code | 60232-2585-4 |
| Proprietary Name | Elta MD UV SPF46 |
| Package Description | 4 g in 1 BOTTLE, SPRAY (60232-2585-4) |
| Product NDC | 60232-2585 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | zinc oxide and octinoxate sunscreen |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20100601 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Swiss American Products, Inc. |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 75; 93 |
| Strength Unit | g/1000g; g/1000g |
| Pharmaceutical Classes |
