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LOreal Paris Sublime Sun - 49967-372-01 - (Avobenzone Homosalate Octisalate Octocrylene Oxybenzone)

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Drug Information of LOreal Paris Sublime Sun

Product NDC: 49967-372
Proprietary Name: LOreal Paris Sublime Sun
Non Proprietary Name: Avobenzone Homosalate Octisalate Octocrylene Oxybenzone
Active Ingredient(s): 3.6; 14.4; 6; 8.4; 7.2    g/120g; g/120g; g/120g; g/120g; g/120g & nbsp;   Avobenzone Homosalate Octisalate Octocrylene Oxybenzone
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of LOreal Paris Sublime Sun

Product NDC: 49967-372
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: 20111001

Package Information of LOreal Paris Sublime Sun

Package NDC: 49967-372-01
Package Description: 120 g in 1 BOTTLE (49967-372-01)

NDC Information of LOreal Paris Sublime Sun

NDC Code 49967-372-01
Proprietary Name LOreal Paris Sublime Sun
Package Description 120 g in 1 BOTTLE (49967-372-01)
Product NDC 49967-372
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Avobenzone Homosalate Octisalate Octocrylene Oxybenzone
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20111001
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name L'Oreal USA Products Inc
Substance Name AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Strength Number 3.6; 14.4; 6; 8.4; 7.2
Strength Unit g/120g; g/120g; g/120g; g/120g; g/120g
Pharmaceutical Classes

Complete Information of LOreal Paris Sublime Sun


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