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 |