| Product NDC: | 75936-122 |
| Proprietary Name: | CC Daily Correct Broad Spectrum SPF 35 Sunscreen |
| Non Proprietary Name: | Titanium DIoxide, Zinc Oxide |
| Active Ingredient(s): | 14.2; 200 mg/mL; mg/mL & nbsp; Titanium DIoxide, Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 75936-122 |
| Labeler Name: | TAYLOR JAMES, LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130107 |
| Package NDC: | 75936-122-02 |
| Package Description: | 1 TUBE in 1 CARTON (75936-122-02) > 47 mL in 1 TUBE (75936-122-01) |
| NDC Code | 75936-122-02 |
| Proprietary Name | CC Daily Correct Broad Spectrum SPF 35 Sunscreen |
| Package Description | 1 TUBE in 1 CARTON (75936-122-02) > 47 mL in 1 TUBE (75936-122-01) |
| Product NDC | 75936-122 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium DIoxide, Zinc Oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130107 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | TAYLOR JAMES, LTD. |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 14.2; 200 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |