La Prairie - 76157-301-13 - (Avobenzone, Octinoxate, Octisalate)

Alphabetical Index


Drug Information of La Prairie

Product NDC: 76157-301
Proprietary Name: La Prairie
Non Proprietary Name: Avobenzone, Octinoxate, Octisalate
Active Ingredient(s): 3; 7.5; 5    kg/100kg; kg/100kg; kg/100kg & nbsp;   Avobenzone, Octinoxate, Octisalate
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of La Prairie

Product NDC: 76157-301
Labeler Name: La Prairie Group AG
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20090101

Package Information of La Prairie

Package NDC: 76157-301-13
Package Description: 1 BOTTLE in 1 BOX (76157-301-13) > .05 kg in 1 BOTTLE (76157-301-12)

NDC Information of La Prairie

NDC Code 76157-301-13
Proprietary Name La Prairie
Package Description 1 BOTTLE in 1 BOX (76157-301-13) > .05 kg in 1 BOTTLE (76157-301-12)
Product NDC 76157-301
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Avobenzone, Octinoxate, Octisalate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20090101
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name La Prairie Group AG
Substance Name AVOBENZONE; OCTINOXATE; OCTISALATE
Strength Number 3; 7.5; 5
Strength Unit kg/100kg; kg/100kg; kg/100kg
Pharmaceutical Classes

Complete Information of La Prairie


General Information