NDC 76348-990-01 - FLAWLESS NAILS

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: 76348-990
Requested NDC: 76348-990-01
Package NDCs from labels: 76348-990-01, 76348-990-02
Manufacturer: RENU LABORATORIES, INC. | RENU LABORATORIES
Effective date: 2023-01-05
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
FLAWLESS NAILS - RENU LABORATORIES, INC. \| RENU LABORATORIES	RENU LABORATORIES, INC. \| RENU LABORATORIES	2023-01-05	HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76348-990-02	2025-01-30	C162847	48780-1	2cef2736-7a49-d83d-e063-dadaa90ab31f	Flawless Nails

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76348-990-01	FLAWLESS NAILS	15 mL in 1 BOTTLE, GLASS	SOLUTION	15		1
76348-990-02	FLAWLESS NAILS	1 in 1 BOX	SOLUTION	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76348-990	FLAWLESS NAILS (TOLNAFTATE) SOLUTION [RENU LABORATORIES, INC.]	1	2 package rows	20230411_f1875a4f-fc46-cb91-e053-2995a90addeb.zip

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 42 of 42 · 822 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Aftate Athlete Foot Cream	TOLNAFTATE	Sabel Med LLC	2aa58a66-e00b-74c9-e054-00144ff88e88	2016-11-23	Warnings	Exact identifier unii: 06KB629TKV
Eagle Brand Medicated Roll On Refresh	CAMPHOR, MENTHOL	Borden Company (Private) Limited	567b6820-fb52-630e-e063-6294a90a8bf8	2015-07-01	Warnings	Exact identifier unii: AV092KU4JH

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.