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Elta MD UV Pure
Elta MD UV Pure - 60232-2582-4 - (titanium dioxide and zinc oxide lotion)
Drug Information of Elta MD UV Pure
| Product NDC: | 60232-2582 |
| Proprietary Name: | Elta MD UV Pure |
| Non Proprietary Name: | titanium dioxide and zinc oxide lotion |
| Active Ingredient(s): | 55; 100 g/1000g; g/1000g & nbsp; titanium dioxide and zinc oxide lotion |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Elta MD UV Pure
| Product NDC: | 60232-2582 |
| Labeler Name: | Swiss American Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110801 |
Package Information of Elta MD UV Pure
| Package NDC: | 60232-2582-4 |
| Package Description: | 4 g in 1 BOTTLE (60232-2582-4) |
NDC Information of Elta MD UV Pure
| NDC Code | 60232-2582-4 |
| Proprietary Name | Elta MD UV Pure |
| Package Description | 4 g in 1 BOTTLE (60232-2582-4) |
| Product NDC | 60232-2582 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | titanium dioxide and zinc oxide lotion |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110801 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Swiss American Products, Inc. |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 55; 100 |
| Strength Unit | g/1000g; g/1000g |
| Pharmaceutical Classes |
