| Product NDC: | 59779-000 | 
| Proprietary Name: | CVS SPF 8 | 
| Non Proprietary Name: | OCTINOXATE, OXYBENZONE | 
| Active Ingredient(s): | 5; 2 g/100g; g/100g & nbsp; OCTINOXATE, OXYBENZONE | 
| Administration Route(s): | TOPICAL | 
| Dosage Form(s): | LOTION | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 59779-000 | 
| Labeler Name: | CVS Pharmacy | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part352 | 
| Marketing Category: | OTC MONOGRAPH NOT FINAL | 
| Start Marketing Date: | 20121211 | 
| Package NDC: | 59779-000-17 | 
| Package Description: | 283 g in 1 BOTTLE, PLASTIC (59779-000-17) | 
| NDC Code | 59779-000-17 | 
| Proprietary Name | CVS SPF 8 | 
| Package Description | 283 g in 1 BOTTLE, PLASTIC (59779-000-17) | 
| Product NDC | 59779-000 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | OCTINOXATE, OXYBENZONE | 
| Dosage Form Name | LOTION | 
| Route Name | TOPICAL | 
| Start Marketing Date | 20121211 | 
| Marketing Category Name | OTC MONOGRAPH NOT FINAL | 
| Labeler Name | CVS Pharmacy | 
| Substance Name | OCTINOXATE; OXYBENZONE | 
| Strength Number | 5; 2 | 
| Strength Unit | g/100g; g/100g | 
| Pharmaceutical Classes |