Product NDC: | 61543-7759 |
Proprietary Name: | Solar Sense for Visible Sun Damage Restoration Daily Facial Cream SPF 15 |
Non Proprietary Name: | ZINC OXIDE,OCTINOXATE |
Active Ingredient(s): | 6; 2 mL/100mL; mL/100mL & nbsp; ZINC OXIDE,OCTINOXATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61543-7759 |
Labeler Name: | CCA Industries Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100204 |
Package NDC: | 61543-7759-2 |
Package Description: | 1 JAR in 1 CARTON (61543-7759-2) > 50 mL in 1 JAR |
NDC Code | 61543-7759-2 |
Proprietary Name | Solar Sense for Visible Sun Damage Restoration Daily Facial Cream SPF 15 |
Package Description | 1 JAR in 1 CARTON (61543-7759-2) > 50 mL in 1 JAR |
Product NDC | 61543-7759 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ZINC OXIDE,OCTINOXATE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20100204 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | CCA Industries Inc |
Substance Name | OCTINOXATE; ZINC OXIDE |
Strength Number | 6; 2 |
Strength Unit | mL/100mL; mL/100mL |
Pharmaceutical Classes |