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Fresh Umbrian Clay Freshface Foundation SPF 20 Sun Empress - 49817-1991-5 - (Octinoxate)

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Drug Information of Fresh Umbrian Clay Freshface Foundation SPF 20 Sun Empress

Product NDC: 49817-1991
Proprietary Name: Fresh Umbrian Clay Freshface Foundation SPF 20 Sun Empress
Non Proprietary Name: Octinoxate
Active Ingredient(s): 3    g/100g & nbsp;   Octinoxate
Administration Route(s): TOPICAL
Dosage Form(s): EMULSION
Coding System: National Drug Codes(NDC)

Labeler Information of Fresh Umbrian Clay Freshface Foundation SPF 20 Sun Empress

Product NDC: 49817-1991
Labeler Name: Guerlain
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20090401

Package Information of Fresh Umbrian Clay Freshface Foundation SPF 20 Sun Empress

Package NDC: 49817-1991-5
Package Description: 1 BOTTLE in 1 CARTON (49817-1991-5) > 33 g in 1 BOTTLE (49817-1991-9)

NDC Information of Fresh Umbrian Clay Freshface Foundation SPF 20 Sun Empress

NDC Code 49817-1991-5
Proprietary Name Fresh Umbrian Clay Freshface Foundation SPF 20 Sun Empress
Package Description 1 BOTTLE in 1 CARTON (49817-1991-5) > 33 g in 1 BOTTLE (49817-1991-9)
Product NDC 49817-1991
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate
Dosage Form Name EMULSION
Route Name TOPICAL
Start Marketing Date 20090401
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Guerlain
Substance Name OCTINOXATE
Strength Number 3
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of Fresh Umbrian Clay Freshface Foundation SPF 20 Sun Empress


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