| 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: | 51414-600-02 |
| Package Description: | 7 g in 1 PACKAGE (51414-600-02) |
| NDC Code | 51414-600-02 |
| Proprietary Name | SPF15 sunscreen |
| Package Description | 7 g in 1 PACKAGE (51414-600-02) |
| 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 |