| Product NDC: | 31190-500 |
| Proprietary Name: | SunScreen SPF30 |
| Non Proprietary Name: | OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE |
| Active Ingredient(s): | 7.5; 2; 4; 2.5 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 31190-500 |
| 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: | 20100422 |
| Package NDC: | 31190-500-60 |
| Package Description: | 1 BOTTLE in 1 CARTON (31190-500-60) > 60 mL in 1 BOTTLE |
| NDC Code | 31190-500-60 |
| Proprietary Name | SunScreen SPF30 |
| Package Description | 1 BOTTLE in 1 CARTON (31190-500-60) > 60 mL in 1 BOTTLE |
| Product NDC | 31190-500 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100422 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Shanghai Kejing Cleaning Products Co., Ltd. |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE |
| Strength Number | 7.5; 2; 4; 2.5 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |