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 |