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Neutrogena Ultra Sheer Dry Touch Sunscreen - 10812-283-66 - (Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone)

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Drug Information of Neutrogena Ultra Sheer Dry Touch Sunscreen

Product NDC: 10812-283
Proprietary Name: Neutrogena Ultra Sheer Dry Touch Sunscreen
Non Proprietary Name: Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone
Active Ingredient(s): 30; 150; 50; 45; 60    mg/mL; mg/mL; mg/mL; mg/mL; mg/mL & nbsp;   Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Neutrogena Ultra Sheer Dry Touch Sunscreen

Product NDC: 10812-283
Labeler Name: Neutrogena Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120515

Package Information of Neutrogena Ultra Sheer Dry Touch Sunscreen

Package NDC: 10812-283-66
Package Description: 144 TUBE in 1 TRAY (10812-283-66) > 14 mL in 1 TUBE

NDC Information of Neutrogena Ultra Sheer Dry Touch Sunscreen

NDC Code 10812-283-66
Proprietary Name Neutrogena Ultra Sheer Dry Touch Sunscreen
Package Description 144 TUBE in 1 TRAY (10812-283-66) > 14 mL in 1 TUBE
Product NDC 10812-283
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20120515
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Neutrogena Corporation
Substance Name AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Strength Number 30; 150; 50; 45; 60
Strength Unit mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Neutrogena Ultra Sheer Dry Touch Sunscreen


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