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All Day Moisturizing - 49035-091-30 - (Octinoxate, zinc oxide)

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Drug Information of All Day Moisturizing

Product NDC: 49035-091
Proprietary Name: All Day Moisturizing
Non Proprietary Name: Octinoxate, zinc oxide
Active Ingredient(s): 60; 30    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 Moisturizing

Product NDC: 49035-091
Labeler Name: Wal-Mart Stores, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20060407

Package Information of All Day Moisturizing

Package NDC: 49035-091-30
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (49035-091-30) > 177 mL in 1 BOTTLE, PLASTIC

NDC Information of All Day Moisturizing

NDC Code 49035-091-30
Proprietary Name All Day Moisturizing
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (49035-091-30) > 177 mL in 1 BOTTLE, PLASTIC
Product NDC 49035-091
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate, zinc oxide
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20060407
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Wal-Mart Stores, Inc
Substance Name OCTINOXATE; ZINC OXIDE
Strength Number 60; 30
Strength Unit mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of All Day Moisturizing


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