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Elta MD UV Clear
Elta MD UV Clear - 60232-2500-1 - (zinc oxide and octinoxate lotion)
Drug Information of Elta MD UV Clear
| Product NDC: | 60232-2500 |
| Proprietary Name: | Elta MD UV Clear |
| Non Proprietary Name: | zinc oxide and octinoxate lotion |
| Active Ingredient(s): | 75; 90 g/1000g; g/1000g & nbsp; zinc oxide and octinoxate lotion |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Elta MD UV Clear
| Product NDC: | 60232-2500 |
| Labeler Name: | Swiss American Products,Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090701 |
Package Information of Elta MD UV Clear
| Package NDC: | 60232-2500-1 |
| Package Description: | 1.7 g in 1 BOTTLE, PUMP (60232-2500-1) |
NDC Information of Elta MD UV Clear
| NDC Code | 60232-2500-1 |
| Proprietary Name | Elta MD UV Clear |
| Package Description | 1.7 g in 1 BOTTLE, PUMP (60232-2500-1) |
| Product NDC | 60232-2500 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | zinc oxide and octinoxate lotion |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20090701 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Swiss American Products,Inc. |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 75; 90 |
| Strength Unit | g/1000g; g/1000g |
| Pharmaceutical Classes |
