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NOEVIR N5
NOEVIR N5 - 62908-012-02 - (ZINC OXIDE, OCTINOXATE, TITANIUM DIOXIDE)
Drug Information of NOEVIR N5
| Product NDC: | 62908-012 |
| Proprietary Name: | NOEVIR N5 |
| Non Proprietary Name: | ZINC OXIDE, OCTINOXATE, TITANIUM DIOXIDE |
| Active Ingredient(s): | 2000; 13800; 144 mg/100g; mg/100g; mg/100g & nbsp; ZINC OXIDE, OCTINOXATE, TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NOEVIR N5
| Product NDC: | 62908-012 |
| Labeler Name: | NOEVIR USA INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100101 |
Package Information of NOEVIR N5
| Package NDC: | 62908-012-02 |
| Package Description: | 1 TRAY in 1 BOX (62908-012-02) > 12 g in 1 TRAY (62908-012-01) |
NDC Information of NOEVIR N5
| NDC Code | 62908-012-02 |
| Proprietary Name | NOEVIR N5 |
| Package Description | 1 TRAY in 1 BOX (62908-012-02) > 12 g in 1 TRAY (62908-012-01) |
| Product NDC | 62908-012 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ZINC OXIDE, OCTINOXATE, TITANIUM DIOXIDE |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | NOEVIR USA INC |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 2000; 13800; 144 |
| Strength Unit | mg/100g; mg/100g; mg/100g |
| Pharmaceutical Classes |
