| Product NDC: | 59779-602 |
| Proprietary Name: | CVS PHARMACY |
| Non Proprietary Name: | AVOBENZONE, OCTINOXATE, OCTISALATE |
| Active Ingredient(s): | 30; 75; 20 mg/mL; mg/mL; mg/mL & nbsp; AVOBENZONE, OCTINOXATE, OCTISALATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 59779-602 |
| Labeler Name: | CVS PHARMACY |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130610 |
| Package NDC: | 59779-602-00 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (59779-602-00) > 118 mL in 1 BOTTLE, PLASTIC (59779-602-04) |
| NDC Code | 59779-602-00 |
| Proprietary Name | CVS PHARMACY |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (59779-602-00) > 118 mL in 1 BOTTLE, PLASTIC (59779-602-04) |
| Product NDC | 59779-602 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, OCTINOXATE, OCTISALATE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130610 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | CVS PHARMACY |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE |
| Strength Number | 30; 75; 20 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |