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Kiehls Since 1851 CrossTerrain UV Skin Protector - 49967-382-01 - (Avobenzone Homosalate Octisalate Octocrylene Oxybenzone)

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Drug Information of Kiehls Since 1851 CrossTerrain UV Skin Protector

Product NDC: 49967-382
Proprietary Name: Kiehls Since 1851 CrossTerrain UV Skin Protector
Non Proprietary Name: Avobenzone Homosalate Octisalate Octocrylene Oxybenzone
Active Ingredient(s): 1.2; 4; 2; 3; 2    g/40g; g/40g; g/40g; g/40g; g/40g & nbsp;   Avobenzone Homosalate Octisalate Octocrylene Oxybenzone
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Kiehls Since 1851 CrossTerrain UV Skin Protector

Product NDC: 49967-382
Labeler Name: L'Oreal USA Products Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100601

Package Information of Kiehls Since 1851 CrossTerrain UV Skin Protector

Package NDC: 49967-382-01
Package Description: 40 g in 1 JAR (49967-382-01)

NDC Information of Kiehls Since 1851 CrossTerrain UV Skin Protector

NDC Code 49967-382-01
Proprietary Name Kiehls Since 1851 CrossTerrain UV Skin Protector
Package Description 40 g in 1 JAR (49967-382-01)
Product NDC 49967-382
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Avobenzone Homosalate Octisalate Octocrylene Oxybenzone
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20100601
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name L'Oreal USA Products Inc
Substance Name AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Strength Number 1.2; 4; 2; 3; 2
Strength Unit g/40g; g/40g; g/40g; g/40g; g/40g
Pharmaceutical Classes

Complete Information of Kiehls Since 1851 CrossTerrain UV Skin Protector


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