| 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 |