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 |