Product NDC: | 51346-002 |
Proprietary Name: | TRUFFLE EX SUN |
Non Proprietary Name: | OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE |
Active Ingredient(s): | 3.75; 2.5; 1.25; 2.4 g/50mL; g/50mL; g/50mL; g/50mL & nbsp; OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51346-002 |
Labeler Name: | NATURE REPUBLIC CO., LTD. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120301 |
Package NDC: | 51346-002-01 |
Package Description: | 50 mL in 1 CARTON (51346-002-01) |
NDC Code | 51346-002-01 |
Proprietary Name | TRUFFLE EX SUN |
Package Description | 50 mL in 1 CARTON (51346-002-01) |
Product NDC | 51346-002 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120301 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | NATURE REPUBLIC CO., LTD. |
Substance Name | OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 3.75; 2.5; 1.25; 2.4 |
Strength Unit | g/50mL; g/50mL; g/50mL; g/50mL |
Pharmaceutical Classes |