| Product NDC: | 61543-7770 |
| Proprietary Name: | Solar Sense Sun Damage Restoration Body 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): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 61543-7770 |
| Labeler Name: | CCA Industries, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101002 |
| Package NDC: | 61543-7770-5 |
| Package Description: | 1 JAR in 1 PACKAGE (61543-7770-5) > 150 mL in 1 JAR |
| NDC Code | 61543-7770-5 |
| Proprietary Name | Solar Sense Sun Damage Restoration Body SPF 15 |
| Package Description | 1 JAR in 1 PACKAGE (61543-7770-5) > 150 mL in 1 JAR |
| Product NDC | 61543-7770 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ZINC OXIDE, OCTINOXATE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20101002 |
| 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 |