enfuselle BODY SUNSCREEN BROAD SPECTRUM SPF 30 (Shaklee Corporation)


Welcome to the PulseAid listing for the enfuselle BODY SUNSCREEN BROAD SPECTRUM SPF 30 drug offered from Shaklee Corporation. 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: Shaklee Corporation
NON-PROPRIETARY NAME: HOMOSALATE, OCTISALATE, AVOBENZONE, and OCTOCRYLENE
SUBSTANCE NAME: OCTISALATE; AVOBENZONE; OCTOCRYLENE; HOMOSALATE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: LOTION
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2013-11-11
END MARKETING DATE: 0000-00-00


enfuselle BODY SUNSCREEN BROAD SPECTRUM SPF 30 HUMAN OTC DRUG Details:

Item Descriptionenfuselle BODY SUNSCREEN BROAD SPECTRUM SPF 30 from Shaklee Corporation
LABELER NAME: Shaklee Corporation
DEA SCHEDULE:
ACTIVE STRENGTH: 50; 30; 100; 100(mg/mL; mg/mL; mg/mL; mg/mL)
START MARKETING DATE: 2013-11-11
END MARKETING DATE: 0000-00-00
PRODUCT ID: 59899-007_4052e240-04fa-0717-e054-00144ff88e88
PRODUCT NDC: 59899-007
APPLICATION NUMBER: part352

Other OCTISALATE; AVOBENZONE; OCTOCRYLENE; HOMOSALATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
CLINIQUE LABORATORIES INC.YOUTH SURGE
Rodan and FieldsRodan and Fields Redefine AM
Shaklee Corporationenfuselle BODY SUNSCREEN BROAD SPECTRUM SPF 30