DAY HYDRATORSPF-15 (220 Laboratories Inc.)


Welcome to the PulseAid listing for the DAY HYDRATOR 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: OCTINOXATE and OCTISALATE and OXYBENZONE
SUBSTANCE NAME: OCTINOXATE; OCTISALATE; OXYBENZONE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: LOTION
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2006-02-01
END MARKETING DATE: 0000-00-00


DAY HYDRATOR SPF-15 HUMAN OTC DRUG Details:

Item DescriptionDAY HYDRATOR SPF-15 from 220 Laboratories Inc.
LABELER NAME: 220 Laboratories Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 75; 50; 30(mg/g; mg/g; mg/g)
START MARKETING DATE: 2006-02-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 57367-027_de535765-6fa3-4715-9dcc-037f6dc80577
PRODUCT NDC: 57367-027
APPLICATION NUMBER: part352

Other OCTINOXATE; OCTISALATE; OXYBENZONE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
220 Laboratories Inc.DAY HYDRATOR
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Prime Enterprises, Inc.Panama Jack
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Tropical Seas, Inc.Reef Safe SPF 15
Valeant Pharmaceuticals North America LLCPurpose
Ventura Corporation Ltd. (San Juan, P.R)LBEL
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Ventura International LTDLBel Paris
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VENTURA INTERNATIONAL LTD.,LBel
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