Home NDC 35781-0500 NDC 35781-0500 - WPR Plus 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 35781-0500
Package NDCs from labels 35781-0500-3, 35781-0500-1, 35781-0500-9
Manufacturer International Brand Management, LLC | Gensco Laboratories, LLC
Effective date 2018-07-17
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type WPR Plus - International Brand Management, LLC | Gensco Laboratories, LLC International Brand Management, LLC | Gensco Laboratories, LLC 2018-07-17 HUMAN PRESCRIPTION DRUG LABEL WPR Plus - International Brand Management, LLC International Brand Management, LLC 2018-07-17 HUMAN OTC DRUG LABEL Lidocaine Hydrochloride - Gensco Laboratories, LLC Gensco Laboratories, LLC 2015-10-01 HUMAN PRESCRIPTION DRUG LABEL
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 35781-0500-3 WPR Plus 30 g in 1 TUBE 30 g 40 mg in 1g 2 35781-0500-1 Lidocaine Hydrochloride 15 g in 1 TUBE GEL 15 1 35781-0500-1 Lidocaine Hydrochloride 1 in 1 CARTON GEL 1 1 35781-0500-3 WPR Plus 30 g in 1 TUBE 30 g 40 mg in 1g 1 35781-0500-3 Lidocaine Hydrochloride 1 in 1 CARTON GEL 1 1 35781-0500-3 Lidocaine Hydrochloride 30 g in 1 TUBE GEL 30 1 35781-0500-9 Lidocaine Hydrochloride 1 in 1 CARTON GEL 1 1 35781-0500-9 Lidocaine Hydrochloride 90 g in 1 TUBE GEL 90 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 35781-0500 WPR PLUS () KIT [INTERNATIONAL BRAND MANAGEMENT, LLC] 2 Unmatched 20180801_9d830535-2202-482d-9d1a-bccd7bbba855.zip 35781-0500 LIDOCAINE HYDROCHLORIDE (LIDOCAINE) GEL [GENSCO LABORATORIES, LLC] 1 6 package rows 20151028_88dbd438-02c0-481a-bdb7-8b3f3c41fd46.zip 35781-0500 WPR PLUS () KIT [INTERNATIONAL BRAND MANAGEMENT, LLC] 1 Unmatched 20180717_793d6fad-31a7-4b28-8395-73825bc18508.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded LIDOCAINE ACTIVE INGREDIENT 98PI200987 LIDOCAINE HYDROCHLORIDE (LIDOCAINE) GEL [GENSCO LABORATORIES, LLC] 1 LIDOCAINE ACTIVE MOIETY 98PI200987 LIDOCAINE HYDROCHLORIDE (LIDOCAINE) GEL [GENSCO LABORATORIES, LLC] 1 FILIPENDULA ULMARIA FLOWER INACTIVE INGREDIENT 06L18L32G6 LIDOCAINE HYDROCHLORIDE (LIDOCAINE) GEL [GENSCO LABORATORIES, LLC] 1 POLYETHYLENE GLYCOL 3350 INACTIVE INGREDIENT G2M7P15E5P LIDOCAINE HYDROCHLORIDE (LIDOCAINE) GEL [GENSCO LABORATORIES, LLC] 1 POLYETHYLENE GLYCOL 400 INACTIVE INGREDIENT B697894SGQ LIDOCAINE HYDROCHLORIDE (LIDOCAINE) GEL [GENSCO LABORATORIES, LLC] 1 QUERCUS ALBA WOOD INACTIVE INGREDIENT XR6BC2ZUAM LIDOCAINE HYDROCHLORIDE (LIDOCAINE) GEL [GENSCO LABORATORIES, LLC] 1 WATER INACTIVE INGREDIENT 059QF0KO0R LIDOCAINE HYDROCHLORIDE (LIDOCAINE) GEL [GENSCO LABORATORIES, LLC] 1 ZINC ACETATE INACTIVE INGREDIENT FM5526K07A LIDOCAINE HYDROCHLORIDE (LIDOCAINE) GEL [GENSCO LABORATORIES, LLC] 1
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 79 of 201 · 4,013 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.