SUNSCREENWATER RESISTANT (220 Laboratories Inc)
Welcome to the PulseAid listing for the SUNSCREEN drug offered from 220 Laboratories 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: | 220 Laboratories Inc |
NON-PROPRIETARY NAME: | HOMOSALATE OXYBENZONE OCTISALATE AVOBENZONE OCTYLCRYLENE |
SUBSTANCE NAME: | HOMOSALATE; OXYBENZONE; OCTISALATE; AVOBENZONE; OCTOCRYLENE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | AEROSOL, SPRAY |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2010-05-10 |
END MARKETING DATE: | 0000-00-00 |
SUNSCREEN WATER RESISTANT HUMAN OTC DRUG Details:
Item Description | SUNSCREEN WATER RESISTANT from 220 Laboratories Inc |
LABELER NAME: | 220 Laboratories Inc |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 150; 50; 50; 30; 20(mg/g; mg/g; mg/g; mg/g; mg/g) |
START MARKETING DATE: | 2010-05-10 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 57367-029_b0602558-795b-4916-b143-74d0e6e6a84c |
PRODUCT NDC: | 57367-029 |
APPLICATION NUMBER: | part352 |
Other HOMOSALATE; OXYBENZONE; OCTISALATE; AVOBENZONE; OCTOCRYLENE Pharmaceutical Manufacturers / Labelers: