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La Prairie Switzerland - 68807-301-11 - (Avobenzone, Octinoxate, Octisalate)

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Drug Information of La Prairie Switzerland

Product NDC: 68807-301
Proprietary Name: La Prairie Switzerland
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 Switzerland

Product NDC: 68807-301
Labeler Name: Temmentec Ag
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20090101

Package Information of La Prairie Switzerland

Package NDC: 68807-301-11
Package Description: 78.4 kg in 1 DRUM (68807-301-11)

NDC Information of La Prairie Switzerland

NDC Code 68807-301-11
Proprietary Name La Prairie Switzerland
Package Description 78.4 kg in 1 DRUM (68807-301-11)
Product NDC 68807-301
Product Type Name HUMAN PRESCRIPTION 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 Temmentec 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 Switzerland


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