Product NDC: | 59779-317 |
Proprietary Name: | CVS DRY SKIN THERAPY WITH SPF 15 |
Non Proprietary Name: | ENSULIZOLE, OCTISALATE AND OCTOCRYLENE |
Active Ingredient(s): | 10; 40; 10 mg/mL; mg/mL; mg/mL & nbsp; ENSULIZOLE, OCTISALATE AND OCTOCRYLENE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59779-317 |
Labeler Name: | CVS Pharmacy |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100719 |
Package NDC: | 59779-317-49 |
Package Description: | 400 mL in 1 BOTTLE, PUMP (59779-317-49) |
NDC Code | 59779-317-49 |
Proprietary Name | CVS DRY SKIN THERAPY WITH SPF 15 |
Package Description | 400 mL in 1 BOTTLE, PUMP (59779-317-49) |
Product NDC | 59779-317 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ENSULIZOLE, OCTISALATE AND OCTOCRYLENE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20100719 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | CVS Pharmacy |
Substance Name | ENSULIZOLE; OCTISALATE; OCTOCRYLENE |
Strength Number | 10; 40; 10 |
Strength Unit | mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |