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Neutrogena Ultra Sheer Dry Touch Sunblock - 10812-366-01 - (Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone)

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Drug Information of Neutrogena Ultra Sheer Dry Touch Sunblock

Product NDC: 10812-366
Proprietary Name: Neutrogena Ultra Sheer Dry Touch Sunblock
Non Proprietary Name: Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone
Active Ingredient(s): 30; 150; 50; 100; 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 Sunblock

Product NDC: 10812-366
Labeler Name: Neutrogena Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100401

Package Information of Neutrogena Ultra Sheer Dry Touch Sunblock

Package NDC: 10812-366-01
Package Description: 88 mL in 1 TUBE (10812-366-01)

NDC Information of Neutrogena Ultra Sheer Dry Touch Sunblock

NDC Code 10812-366-01
Proprietary Name Neutrogena Ultra Sheer Dry Touch Sunblock
Package Description 88 mL in 1 TUBE (10812-366-01)
Product NDC 10812-366
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 20100401
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Neutrogena Corporation
Substance Name AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Strength Number 30; 150; 50; 100; 60
Strength Unit mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Neutrogena Ultra Sheer Dry Touch Sunblock


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