Home > National Drug Code (NDC) > Elizabeth Arden Moisture Shield SPF 15

Elizabeth Arden Moisture Shield SPF 15 - 67938-0801-1 - (Octinoxate)

Alphabetical Index


Drug Information of Elizabeth Arden Moisture Shield SPF 15

Product NDC: 67938-0801
Proprietary Name: Elizabeth Arden Moisture Shield SPF 15
Non Proprietary Name: Octinoxate
Active Ingredient(s): .75; 3.125; 2.5; 1    mL/50mL; mL/50mL; mL/50mL; mL/50mL & nbsp;   Octinoxate
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Elizabeth Arden Moisture Shield SPF 15

Product NDC: 67938-0801
Labeler Name: Elizabeth Arden, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20060626

Package Information of Elizabeth Arden Moisture Shield SPF 15

Package NDC: 67938-0801-1
Package Description: 1 BOTTLE, PUMP in 1 BOX (67938-0801-1) > 50 mL in 1 BOTTLE, PUMP (67938-0801-2)

NDC Information of Elizabeth Arden Moisture Shield SPF 15

NDC Code 67938-0801-1
Proprietary Name Elizabeth Arden Moisture Shield SPF 15
Package Description 1 BOTTLE, PUMP in 1 BOX (67938-0801-1) > 50 mL in 1 BOTTLE, PUMP (67938-0801-2)
Product NDC 67938-0801
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20060626
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Elizabeth Arden, Inc
Substance Name AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE
Strength Number .75; 3.125; 2.5; 1
Strength Unit mL/50mL; mL/50mL; mL/50mL; mL/50mL
Pharmaceutical Classes

Complete Information of Elizabeth Arden Moisture Shield SPF 15


General Information