| Product NDC: | 62908-011 |
| Proprietary Name: | NOEVIR RAYSELA |
| Non Proprietary Name: | ZINC OXIDE, OCTINOXATE, TITANIUM DIOXIDE |
| Active Ingredient(s): | 7500; 2070; 14250 mg/100g; mg/100g; mg/100g & nbsp; ZINC OXIDE, OCTINOXATE, TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 62908-011 |
| Labeler Name: | NOEVIR USA INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100101 |
| Package NDC: | 62908-011-02 |
| Package Description: | 1 TUBE in 1 BOX (62908-011-02) > 35 g in 1 TUBE (62908-011-01) |
| NDC Code | 62908-011-02 |
| Proprietary Name | NOEVIR RAYSELA |
| Package Description | 1 TUBE in 1 BOX (62908-011-02) > 35 g in 1 TUBE (62908-011-01) |
| Product NDC | 62908-011 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ZINC OXIDE, OCTINOXATE, TITANIUM DIOXIDE |
| Dosage Form Name | CREAM |
| 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 | 7500; 2070; 14250 |
| Strength Unit | mg/100g; mg/100g; mg/100g |
| Pharmaceutical Classes |