Product NDC: | 51346-028 |
Proprietary Name: | MANGO BEBE LIP ESSENCE |
Non Proprietary Name: | OCTINOXATE, OCTISALATE |
Active Ingredient(s): | .6; .3 g/10mL; g/10mL & nbsp; OCTINOXATE, OCTISALATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51346-028 |
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: | 51346-028-01 |
Package Description: | 10 mL in 1 CARTON (51346-028-01) |
NDC Code | 51346-028-01 |
Proprietary Name | MANGO BEBE LIP ESSENCE |
Package Description | 10 mL in 1 CARTON (51346-028-01) |
Product NDC | 51346-028 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OCTISALATE |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20120301 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | NATURE REPUBLIC CO., LTD. |
Substance Name | OCTINOXATE; OCTISALATE |
Strength Number | .6; .3 |
Strength Unit | g/10mL; g/10mL |
Pharmaceutical Classes |