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Neova DNA Damage Control - Active
Neova DNA Damage Control - Active - 62362-129-03 - (Zinc Oxide, Octinoxate, Octisalate)
Drug Information of Neova DNA Damage Control - Active
| Product NDC: | 62362-129 |
| Proprietary Name: | Neova DNA Damage Control - Active |
| Non Proprietary Name: | Zinc Oxide, Octinoxate, Octisalate |
| Active Ingredient(s): | 7.5; 3; 8 mL/100mL; mL/100mL; mL/100mL & nbsp; Zinc Oxide, Octinoxate, Octisalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Neova DNA Damage Control - Active
| Product NDC: | 62362-129 |
| Labeler Name: | PhotoMedex, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120105 |
Package Information of Neova DNA Damage Control - Active
| Package NDC: | 62362-129-03 |
| Package Description: | 1 PACKAGE in 1 POUCH (62362-129-03) > 2 mL in 1 PACKAGE (62362-129-02) |
NDC Information of Neova DNA Damage Control - Active
| NDC Code | 62362-129-03 |
| Proprietary Name | Neova DNA Damage Control - Active |
| Package Description | 1 PACKAGE in 1 POUCH (62362-129-03) > 2 mL in 1 PACKAGE (62362-129-02) |
| Product NDC | 62362-129 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide, Octinoxate, Octisalate |
| Dosage Form Name | EMULSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120105 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | PhotoMedex, Inc. |
| Substance Name | OCTINOXATE; OCTISALATE; ZINC OXIDE |
| Strength Number | 7.5; 3; 8 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
