Product NDC: | 59779-020 |
Proprietary Name: | CVS Pharmacy Sunscreen SPF 45 |
Non Proprietary Name: | OCTINOXATE, OCTOCRLYENE, ZINC OXIDE |
Active Ingredient(s): | 7.5; 8; 6.8 g/100g; g/100g; g/100g & nbsp; OCTINOXATE, OCTOCRLYENE, ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59779-020 |
Labeler Name: | CVS Pharmacy |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20121217 |
Package NDC: | 59779-020-23 |
Package Description: | 113 g in 1 BOTTLE, PLASTIC (59779-020-23) |
NDC Code | 59779-020-23 |
Proprietary Name | CVS Pharmacy Sunscreen SPF 45 |
Package Description | 113 g in 1 BOTTLE, PLASTIC (59779-020-23) |
Product NDC | 59779-020 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OCTOCRLYENE, ZINC OXIDE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20121217 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | CVS Pharmacy |
Substance Name | OCTINOXATE; OCTOCRYLENE; ZINC OXIDE |
Strength Number | 7.5; 8; 6.8 |
Strength Unit | g/100g; g/100g; g/100g |
Pharmaceutical Classes |