DAYWEAR - 11559-008-01 - (OCTISALATE, AVOBENZONE)

Alphabetical Index


Drug Information of DAYWEAR

Product NDC: 11559-008
Proprietary Name: DAYWEAR
Non Proprietary Name: OCTISALATE, AVOBENZONE
Active Ingredient(s): 3; 5    mL/100mL; mL/100mL & nbsp;   OCTISALATE, AVOBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of DAYWEAR

Product NDC: 11559-008
Labeler Name: ESTEE LAUDER INC
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100901

Package Information of DAYWEAR

Package NDC: 11559-008-01
Package Description: 1 TUBE in 1 TUBE (11559-008-01) > 50 mL in 1 TUBE (11559-008-02)

NDC Information of DAYWEAR

NDC Code 11559-008-01
Proprietary Name DAYWEAR
Package Description 1 TUBE in 1 TUBE (11559-008-01) > 50 mL in 1 TUBE (11559-008-02)
Product NDC 11559-008
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTISALATE, AVOBENZONE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20100901
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name ESTEE LAUDER INC
Substance Name AVOBENZONE; OCTISALATE
Strength Number 3; 5
Strength Unit mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of DAYWEAR


General Information