Avon Sun - 10096-0296-1 - (Homosalate, Octinoxate, Octisalate, Oxybenzone, Avobenzone, Octocrylene)

Alphabetical Index


Drug Information of Avon Sun

Product NDC: 10096-0296
Proprietary Name: Avon Sun
Non Proprietary Name: Homosalate, Octinoxate, Octisalate, Oxybenzone, Avobenzone, Octocrylene
Active Ingredient(s): 28.5; 80; 75; 47.5; 25.6; 47.5    mg/g; mg/g; mg/g; mg/g; mg/g; mg/g & nbsp;   Homosalate, Octinoxate, Octisalate, Oxybenzone, Avobenzone, Octocrylene
Administration Route(s): TOPICAL
Dosage Form(s): AEROSOL, SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of Avon Sun

Product NDC: 10096-0296
Labeler Name: Avon Products, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130326

Package Information of Avon Sun

Package NDC: 10096-0296-1
Package Description: 136.5 g in 1 BOTTLE, SPRAY (10096-0296-1)

NDC Information of Avon Sun

NDC Code 10096-0296-1
Proprietary Name Avon Sun
Package Description 136.5 g in 1 BOTTLE, SPRAY (10096-0296-1)
Product NDC 10096-0296
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Homosalate, Octinoxate, Octisalate, Oxybenzone, Avobenzone, Octocrylene
Dosage Form Name AEROSOL, SPRAY
Route Name TOPICAL
Start Marketing Date 20130326
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Avon Products, Inc
Substance Name AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Strength Number 28.5; 80; 75; 47.5; 25.6; 47.5
Strength Unit mg/g; mg/g; mg/g; mg/g; mg/g; mg/g
Pharmaceutical Classes

Complete Information of Avon Sun


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