Product NDC: | 51414-600 |
Proprietary Name: | SPF15 sunscreen |
Non Proprietary Name: | Octinoxate,oxybenzone,OCTISALATE |
Active Ingredient(s): | 4; 2; 4 g/100g; g/100g; g/100g & nbsp; Octinoxate,oxybenzone,OCTISALATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51414-600 |
Labeler Name: | Yuyao Jessie Commodity Co.,Ltd. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120912 |
Package NDC: | 51414-600-21 |
Package Description: | 180 g in 1 PACKAGE (51414-600-21) |
NDC Code | 51414-600-21 |
Proprietary Name | SPF15 sunscreen |
Package Description | 180 g in 1 PACKAGE (51414-600-21) |
Product NDC | 51414-600 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate,oxybenzone,OCTISALATE |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20120912 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Yuyao Jessie Commodity Co.,Ltd. |
Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 4; 2; 4 |
Strength Unit | g/100g; g/100g; g/100g |
Pharmaceutical Classes |