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Kiehls Since 1851 Dermatologist Solutions - 49967-707-01 - (Avobenzone Homosalate Octisalate Octocrylene Oxybenzone)

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Drug Information of Kiehls Since 1851 Dermatologist Solutions

Product NDC: 49967-707
Proprietary Name: Kiehls Since 1851 Dermatologist Solutions
Non Proprietary Name: Avobenzone Homosalate Octisalate Octocrylene Oxybenzone
Active Ingredient(s): 4.5; 22.5; 7.5; 7.5; 9    mL/150mL; mL/150mL; mL/150mL; mL/150mL; mL/150mL & nbsp;   Avobenzone Homosalate Octisalate Octocrylene Oxybenzone
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Kiehls Since 1851 Dermatologist Solutions

Product NDC: 49967-707
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: 20120601

Package Information of Kiehls Since 1851 Dermatologist Solutions

Package NDC: 49967-707-01
Package Description: 150 mL in 1 BOTTLE, PLASTIC (49967-707-01)

NDC Information of Kiehls Since 1851 Dermatologist Solutions

NDC Code 49967-707-01
Proprietary Name Kiehls Since 1851 Dermatologist Solutions
Package Description 150 mL in 1 BOTTLE, PLASTIC (49967-707-01)
Product NDC 49967-707
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Avobenzone Homosalate Octisalate Octocrylene Oxybenzone
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20120601
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name L'Oreal USA Products Inc
Substance Name AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Strength Number 4.5; 22.5; 7.5; 7.5; 9
Strength Unit mL/150mL; mL/150mL; mL/150mL; mL/150mL; mL/150mL
Pharmaceutical Classes

Complete Information of Kiehls Since 1851 Dermatologist Solutions


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