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VITAMIN E DAY - 62874-005-01 - (OCTISALATE, AVOBENZONE)

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Drug Information of VITAMIN E DAY

Product NDC: 62874-005
Proprietary Name: VITAMIN E DAY
Non Proprietary Name: OCTISALATE, AVOBENZONE
Active Ingredient(s): 3; 5    mL/100mL; mL/100mL & nbsp;   OCTISALATE, AVOBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of VITAMIN E DAY

Product NDC: 62874-005
Labeler Name: JO MALONE LTD
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110501

Package Information of VITAMIN E DAY

Package NDC: 62874-005-01
Package Description: 50 mL in 1 JAR (62874-005-01)

NDC Information of VITAMIN E DAY

NDC Code 62874-005-01
Proprietary Name VITAMIN E DAY
Package Description 50 mL in 1 JAR (62874-005-01)
Product NDC 62874-005
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTISALATE, AVOBENZONE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20110501
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name JO MALONE LTD
Substance Name AVOBENZONE; OCTISALATE
Strength Number 3; 5
Strength Unit mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of VITAMIN E DAY


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