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 |