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Natria
Natria - 44717-533-02 - (Ethylhexyl Methoxycinnamate, Zinc Oxide)
Drug Information of Natria
| Product NDC: | 44717-533 |
| Proprietary Name: | Natria |
| Non Proprietary Name: | Ethylhexyl Methoxycinnamate, Zinc Oxide |
| Active Ingredient(s): | 7.5; 2.5 mL/100mL; mL/100mL & nbsp; Ethylhexyl Methoxycinnamate, Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Natria
| Product NDC: | 44717-533 |
| Labeler Name: | Wasatch Product Development |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100101 |
Package Information of Natria
| Package NDC: | 44717-533-02 |
| Package Description: | 1 TUBE in 1 BOX (44717-533-02) > 75 mL in 1 TUBE (44717-533-01) |
NDC Information of Natria
| NDC Code | 44717-533-02 |
| Proprietary Name | Natria |
| Package Description | 1 TUBE in 1 BOX (44717-533-02) > 75 mL in 1 TUBE (44717-533-01) |
| Product NDC | 44717-533 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ethylhexyl Methoxycinnamate, Zinc Oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Wasatch Product Development |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 7.5; 2.5 |
| Strength Unit | mL/100mL; mL/100mL |
| Pharmaceutical Classes |
