AveenoUltra-Calming Daily Moisturizer SPF 30 (Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.)


Welcome to the PulseAid listing for the Aveeno drug offered from Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.. This pharmaceutical is classified as a HUMAN OTC DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN OTC DRUG drug type category.
LABELER NAME / MANUFACTURER: Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
NON-PROPRIETARY NAME: Homosalate, Octinoxate, Octisalate and Titanium Dioxide
SUBSTANCE NAME: HOMOSALATE; OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: LOTION
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2009-08-25
END MARKETING DATE: 0000-00-00


Aveeno Ultra-Calming Daily Moisturizer SPF 30 HUMAN OTC DRUG Details:

Item DescriptionAveeno Ultra-Calming Daily Moisturizer SPF 30 from Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
LABELER NAME: Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 51.3; 76.9; 51.3; 24.6(mg/mL; mg/mL; mg/mL; mg/mL)
START MARKETING DATE: 2009-08-25
END MARKETING DATE: 0000-00-00
PRODUCT ID: 58232-0512_edbf98d1-cfa7-49f1-8190-c87daa14ecfe
PRODUCT NDC: 58232-0512
APPLICATION NUMBER: part352

Other HOMOSALATE; OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Beiersdorf IncEucerin Daily Protection Body
Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.Aveeno
Prime Enterprises, Inc.Fair and Square