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EltaMD UV Facial
EltaMD UV Facial - 60232-2283-3 - (Zinc Oxide, Octinoxate)
Drug Information of EltaMD UV Facial
| Product NDC: | 60232-2283 |
| Proprietary Name: | EltaMD UV Facial |
| Non Proprietary Name: | Zinc Oxide, Octinoxate |
| Active Ingredient(s): | 75; 70 g/1000g; g/1000g & nbsp; Zinc Oxide, Octinoxate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of EltaMD UV Facial
| Product NDC: | 60232-2283 |
| Labeler Name: | Swiss-American Products |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20020430 |
Package Information of EltaMD UV Facial
| Package NDC: | 60232-2283-3 |
| Package Description: | 86 g in 1 TUBE (60232-2283-3) |
NDC Information of EltaMD UV Facial
| NDC Code | 60232-2283-3 |
| Proprietary Name | EltaMD UV Facial |
| Package Description | 86 g in 1 TUBE (60232-2283-3) |
| Product NDC | 60232-2283 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide, Octinoxate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20020430 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Swiss-American Products |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 75; 70 |
| Strength Unit | g/1000g; g/1000g |
| Pharmaceutical Classes |
