Aveeno - 58232-0512-1 - (Homosalate, Octinoxate, Octisalate and Titanium Dioxide)

Alphabetical Index


Drug Information of Aveeno

Product NDC: 58232-0512
Proprietary Name: Aveeno
Non Proprietary Name: Homosalate, Octinoxate, Octisalate and Titanium Dioxide
Active Ingredient(s): 51.3; 76.9; 51.3; 24.6    mg/mL; mg/mL; mg/mL; mg/mL & nbsp;   Homosalate, Octinoxate, Octisalate and Titanium Dioxide
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Aveeno

Product NDC: 58232-0512
Labeler Name: Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20090825

Package Information of Aveeno

Package NDC: 58232-0512-1
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (58232-0512-1) > 75 mL in 1 BOTTLE, PLASTIC

NDC Information of Aveeno

NDC Code 58232-0512-1
Proprietary Name Aveeno
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (58232-0512-1) > 75 mL in 1 BOTTLE, PLASTIC
Product NDC 58232-0512
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Homosalate, Octinoxate, Octisalate and Titanium Dioxide
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20090825
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
Substance Name HOMOSALATE; OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE
Strength Number 51.3; 76.9; 51.3; 24.6
Strength Unit mg/mL; mg/mL; mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Aveeno


General Information