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 Description | NO-AD Splash 30 Sunscreen from Sun & Skin Care Research, LLC |
LABELER NAME: | Sun & Skin Care Research, LLC |
DEA SCHEDULE: |
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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: