Home NDC 76348-997 NDC 76348-997 - NAIL RENU Antifungal 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 76348-997
Package NDCs from labels 76348-997-01, 76348-997-02
Manufacturer RENU LABORATORIES, INC.
Effective date 2023-07-24
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type NAIL RENU ANTIFUNGAL CREAM RENU LABORATORIES, INC. 2023-07-24 HUMAN OTC DRUG LABEL
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 76348-997-01 NAIL RENU Antifungal 28 g in 1 TUBE CREAM 28 1 76348-997-02 NAIL RENU Antifungal 1 in 1 BOX CREAM 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76348-997 NAIL RENU ANTIFUNGAL (MICONAZOLE NITRATE 2%) CREAM [RENU LABORATORIES, INC.] 1 2 package rows 20230816_003d6dd9-f805-3185-e063-6394a90afc94.zip