Product NDC: | 31720-303 |
Proprietary Name: | SEPHORA CC Care Color SPF 20 sunscreen |
Non Proprietary Name: | OCTINOXATE, OXYBENZONE |
Active Ingredient(s): | 75; 20 mg/mL; mg/mL & nbsp; OCTINOXATE, OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 31720-303 |
Labeler Name: | S+ |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130606 |
Package NDC: | 31720-303-08 |
Package Description: | 1 BOTTLE in 1 CARTON (31720-303-08) > 30 mL in 1 BOTTLE |
NDC Code | 31720-303-08 |
Proprietary Name | SEPHORA CC Care Color SPF 20 sunscreen |
Package Description | 1 BOTTLE in 1 CARTON (31720-303-08) > 30 mL in 1 BOTTLE |
Product NDC | 31720-303 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OXYBENZONE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20130606 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | S+ |
Substance Name | OCTINOXATE; OXYBENZONE |
Strength Number | 75; 20 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |