Signature Care Athletes Foot Antifungal

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	23667-813	23667-813-01	D	Discontinued by firm		2026-10-05

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

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
23667-813-01	Signature Care Athletes Foot Antifungal	150 g in 1 CAN	LIQUID	150		2

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
23667-813	SIGNATURE CARE ATHLETES FOOT ANTIFUNGAL (TOLNAFTATE) LIQUID [FORMULATED SOLUTIONS, LLC]	2	Legacy NDC, 1 package rows	20231207_46c6362f-2659-36b8-e054-00144ff8d46c.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
06KB629TKV	TOLNAFTATE	2398-96-1	TOLNAFTATE

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
313423	tolnaftate 1 % Topical Solution	PSN	46c6362f-2659-36b8-e054-00144ff8d46c	2
313423	tolnaftate 10 MG/ML Topical Solution	SCD	46c6362f-2659-36b8-e054-00144ff8d46c	2
313423	tolnaftate 1 % Topical Solution	SY	46c6362f-2659-36b8-e054-00144ff8d46c	2

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
23667-813-01	23667081301	150 g in 1 CAN (23667-813-01)	150 g	2017-01-21	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Signature Care Athlete's Foot Tolnaftate Antifungal	Formulated Solutions, LLC	2023-12-02	HUMAN OTC DRUG LABEL	2