Product NDC: | 57817-300 |
Proprietary Name: | SPF 30 Sunscreen |
Non Proprietary Name: | OCTINOXATE OXYBENZONE Octisalate |
Active Ingredient(s): | 6; 5; 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: | 57817-300 |
Labeler Name: | Hangzhou Haorun Technology CO.,LTD. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130418 |
Package NDC: | 57817-300-18 |
Package Description: | 150 g in 1 BOTTLE (57817-300-18) |
NDC Code | 57817-300-18 |
Proprietary Name | SPF 30 Sunscreen |
Package Description | 150 g in 1 BOTTLE (57817-300-18) |
Product NDC | 57817-300 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE OXYBENZONE Octisalate |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20130418 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Hangzhou Haorun Technology CO.,LTD. |
Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 6; 5; 4 |
Strength Unit | g/100g; g/100g; g/100g |
Pharmaceutical Classes |