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La Praire Switzerland - 76157-321-02 - (Avobenzone, Octinoxate, Octisalate)

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Drug Information of La Praire Switzerland

Product NDC: 76157-321
Proprietary Name: La Praire Switzerland
Non Proprietary Name: Avobenzone, Octinoxate, Octisalate
Active Ingredient(s): 3; 7.5; 5    mL/50mL; mL/50mL; mL/50mL & nbsp;   Avobenzone, Octinoxate, Octisalate
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of La Praire Switzerland

Product NDC: 76157-321
Labeler Name: La Prairie Group AG
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110617

Package Information of La Praire Switzerland

Package NDC: 76157-321-02
Package Description: 1 BOTTLE in 1 BOX (76157-321-02) > 50 mL in 1 BOTTLE (76157-321-01)

NDC Information of La Praire Switzerland

NDC Code 76157-321-02
Proprietary Name La Praire Switzerland
Package Description 1 BOTTLE in 1 BOX (76157-321-02) > 50 mL in 1 BOTTLE (76157-321-01)
Product NDC 76157-321
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Avobenzone, Octinoxate, Octisalate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20110617
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 mL/50mL; mL/50mL; mL/50mL
Pharmaceutical Classes

Complete Information of La Praire Switzerland


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