NO-AD Splash 30 Sunscreen (Sun & Skin Care Research, LLC)


Welcome to the PulseAid listing for the NO-AD Splash 30 Sunscreen drug offered from Sun & Skin Care Research, LLC. 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: Sun & Skin Care Research, LLC
NON-PROPRIETARY NAME: avobenzone, homosalate, octisalate, oxybenzone
SUBSTANCE NAME: HOMOSALATE; OCTISALATE; OXYBENZONE; AVOBENZONE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: LOTION
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2012-01-01
END MARKETING DATE: 0000-00-00


NO-AD Splash 30 Sunscreen HUMAN OTC DRUG Details:

Item DescriptionNO-AD Splash 30 Sunscreen from Sun & Skin Care Research, LLC
LABELER NAME: Sun & Skin Care Research, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 10; 5; 3; 2(mL/100mL; mL/100mL; mL/100mL; mL/100mL)
START MARKETING DATE: 2012-01-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 62802-213_53429f50-a195-4769-b3aa-7d493aaa8ac4
PRODUCT NDC: 62802-213
APPLICATION NUMBER: part352

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

Manufacturer / LabelerProprietary Name
Cardinal HealthLeader
Sun & Skin Care Research, LLCNO-AD Splash 30 Sunscreen