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All Day Moisture
All Day Moisture - 59779-909-30 - (Octinoxate, Zinc Oxide)
Drug Information of All Day Moisture
| Product NDC: | 59779-909 |
| Proprietary Name: | All Day Moisture |
| Non Proprietary Name: | Octinoxate, Zinc Oxide |
| Active Ingredient(s): | 61.2; 30.6 mg/mL; mg/mL & nbsp; Octinoxate, Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of All Day Moisture
| Product NDC: | 59779-909 |
| Labeler Name: | CVS Pharmacy |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20050715 |
Package Information of All Day Moisture
| Package NDC: | 59779-909-30 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (59779-909-30) > 177 mL in 1 BOTTLE, PLASTIC |
NDC Information of All Day Moisture
| NDC Code | 59779-909-30 |
| Proprietary Name | All Day Moisture |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (59779-909-30) > 177 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 59779-909 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Zinc Oxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20050715 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CVS Pharmacy |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 61.2; 30.6 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
