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: |
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| 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:
