Home
>
National Drug Code (NDC)
>
All Day Moisture
All Day Moisture - 59779-091-26 - (Octinoxate)
Drug Information of All Day Moisture
| Product NDC: | 59779-091 |
| Proprietary Name: | All Day Moisture |
| Non Proprietary Name: | Octinoxate |
| Active Ingredient(s): | 60; 30 mg/mL; mg/mL & nbsp; Octinoxate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of All Day Moisture
| Product NDC: | 59779-091 |
| Labeler Name: | CVS Pharmacy, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20060228 |
Package Information of All Day Moisture
| Package NDC: | 59779-091-26 |
| Package Description: | 118 BOTTLE, PUMP in 1 CARTON (59779-091-26) > 118 mL in 1 BOTTLE, PUMP |
NDC Information of All Day Moisture
| NDC Code | 59779-091-26 |
| Proprietary Name | All Day Moisture |
| Package Description | 118 BOTTLE, PUMP in 1 CARTON (59779-091-26) > 118 mL in 1 BOTTLE, PUMP |
| Product NDC | 59779-091 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20060228 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | CVS Pharmacy, Inc |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 60; 30 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
