| Product NDC: | 31190-700 |
| Proprietary Name: | SunScreen SPF 30 |
| Non Proprietary Name: | AVOBENZONE,OCTINOXATE, OCTISALATE, OXYBENZONE |
| Active Ingredient(s): | 2; 7.5; 5; 6 g/100g; g/100g; g/100g; g/100g & nbsp; AVOBENZONE,OCTINOXATE, OCTISALATE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 31190-700 |
| Labeler Name: | Shanghai Kejing Cleaning Products Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110901 |
| Package NDC: | 31190-700-17 |
| Package Description: | 1 TUBE in 1 CARTON (31190-700-17) > 17 g in 1 TUBE |
| NDC Code | 31190-700-17 |
| Proprietary Name | SunScreen SPF 30 |
| Package Description | 1 TUBE in 1 CARTON (31190-700-17) > 17 g in 1 TUBE |
| Product NDC | 31190-700 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE,OCTINOXATE, OCTISALATE, OXYBENZONE |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20110901 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Shanghai Kejing Cleaning Products Co., Ltd. |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 2; 7.5; 5; 6 |
| Strength Unit | g/100g; g/100g; g/100g; g/100g |
| Pharmaceutical Classes |