Product NDC: | 51346-214 |
Proprietary Name: | UV LOCK FLOWER WATER GEL SUN |
Non Proprietary Name: | OCTINOXATE, OCTISALATE |
Active Ingredient(s): | 4.8; 2.4 mg/80mL; mg/80mL & nbsp; OCTINOXATE, OCTISALATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51346-214 |
Labeler Name: | NATURE REPUBLIC CO., LTD. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130201 |
Package NDC: | 51346-214-01 |
Package Description: | 80 mL in 1 CARTON (51346-214-01) |
NDC Code | 51346-214-01 |
Proprietary Name | UV LOCK FLOWER WATER GEL SUN |
Package Description | 80 mL in 1 CARTON (51346-214-01) |
Product NDC | 51346-214 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OCTISALATE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20130201 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | NATURE REPUBLIC CO., LTD. |
Substance Name | OCTINOXATE; OCTISALATE |
Strength Number | 4.8; 2.4 |
Strength Unit | mg/80mL; mg/80mL |
Pharmaceutical Classes |