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 the 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 DescriptionSUNSCREEN WATER RESISTANT from 220 Laboratories Inc
LABELER NAME: 220 Laboratories Inc
DEA SCHEDULE:
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:

Manufacturer / LabelerProprietary Name
220 Laboratories IncSUNSCREEN
AMCOL Health & Beauty Solutions, Inc. DBASheltered Broad Spectrum SPF 55 Sunscreen
Avon Products, IncAvon Sun
CVS HealthSkinPharmacy Advanced Sun Therapy Broad Spectrum SPF 50 Face
New Avon LLCAvon Sun