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LOreal Paris Sublime Sun - 49967-359-01 - (Avobenzone Homosalate Octisalate Octocrylene Oxybenzone)

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Drug Information of LOreal Paris Sublime Sun

Product NDC: 49967-359
Proprietary Name: LOreal Paris Sublime Sun
Non Proprietary Name: Avobenzone Homosalate Octisalate Octocrylene Oxybenzone
Active Ingredient(s): 3.75; 18.75; 6.25; 8.75; 8.75    mL/125mL; mL/125mL; mL/125mL; mL/125mL; mL/125mL & nbsp;   Avobenzone Homosalate Octisalate Octocrylene Oxybenzone
Administration Route(s): TOPICAL
Dosage Form(s): AEROSOL, SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of LOreal Paris Sublime Sun

Product NDC: 49967-359
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: 49967-359-01
Package Description: 125 mL in 1 BOTTLE, SPRAY (49967-359-01)

NDC Information of LOreal Paris Sublime Sun

NDC Code 49967-359-01
Proprietary Name LOreal Paris Sublime Sun
Package Description 125 mL in 1 BOTTLE, SPRAY (49967-359-01)
Product NDC 49967-359
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Avobenzone Homosalate Octisalate Octocrylene Oxybenzone
Dosage Form Name AEROSOL, SPRAY
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 3.75; 18.75; 6.25; 8.75; 8.75
Strength Unit mL/125mL; mL/125mL; mL/125mL; mL/125mL; mL/125mL
Pharmaceutical Classes

Complete Information of LOreal Paris Sublime Sun


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