FDA.reportPublic FDA data

NDC 84320-002 - Lucid Hearing Earwax Removal Kit and Bulb

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
84320-002
Package NDCs from labels
84320-002-00
Manufacturer
Hearing Lab Technology LLC | Bell Pharmaceuticals, Inc.
Effective date
2026-05-29
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Lucid Hearing Earwax Removal DropsHearing Lab Technology LLC | Bell Pharmaceuticals, Inc.2026-05-29HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84320-002-00Lucid Hearing Earwax Removal Kit and Bulb15 mL in 1 BOTTLESOLUTION/ DROPS15 mL65 mg in 1mL1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84320-002LUCID HEARING EARWAX REMOVAL KIT AND BULB (CARBAMIDE PEROXIDE) KIT [HEARING LAB TECHNOLOGY LLC]1Unmatched20240517_5e09f566-397f-44d6-8ba2-90987765c737.zip