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All Day Moisture - 59779-909-30 - (Octinoxate, Zinc Oxide)

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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

Complete Information of All Day Moisture


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