Lubriderm Daily MoistureSunscreen Broad Spectrum SPF15 (Johnson & Johnson Consumer Inc.)
Welcome to the PulseAid listing for the Lubriderm Daily Moisture drug offered from Johnson & Johnson Consumer 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: | Johnson & Johnson Consumer Inc. |
NON-PROPRIETARY NAME: | Avobenzone, Octisalate, Octocrylene, and Oxybenzone |
SUBSTANCE NAME: | AVOBENZONE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | LOTION |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2010-07-01 |
END MARKETING DATE: | 2019-08-01 |
Lubriderm Daily Moisture Sunscreen Broad Spectrum SPF15 HUMAN OTC DRUG Details:
Item Description | Lubriderm Daily Moisture Sunscreen Broad Spectrum SPF15 from Johnson & Johnson Consumer Inc. |
LABELER NAME: | Johnson & Johnson Consumer Inc. |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 20; 40; 30; 22(mg/mL; mg/mL; mg/mL; mg/mL) |
START MARKETING DATE: | 2010-07-01 |
END MARKETING DATE: | 2019-08-01 |
PRODUCT ID: | 58232-0753_972194c3-345b-47b6-9b10-00d1af77a0bd |
PRODUCT NDC: | 58232-0753 |
APPLICATION NUMBER: | part352 |
Other AVOBENZONE; OCTISALATE; OCTOCRYLENE; OXYBENZONE Pharmaceutical Manufacturers / Labelers: