Tolnaftate

Product NDC: 11673-091
11-digit product format: 116730091
Labeler code: 11673
Product ID: 11673-091_c77bedd9-a377-3845-e053-2995a90ac7e3
Type: HUMAN OTC DRUG
Nonproprietary name: Antifungal Liquid Maximum Strength
Dosage form: LIQUID
Route: TOPICAL
Labeler: Target Corporation
Application: part333C
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2021-02-15
Marketing end: 0000-00-00
Substance: TOLNAFTATE
Active strength: 0 g/30mL
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	11673-091		D	Discontinued by firm		2026-10-05
excluded package	package	11673-091	11673-091-01	D	Discontinued by firm		2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 4 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	11673-091-01	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	11673-091-01	`f5e01cc5f278…`	`a2eaf40c39c3…`

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
11673-091-01	2023-01-31	C162847	48780-1	f386c64a-4421-0266-e053-dadaa90a7c1a	Target Tolnaftate 1% Anti-Fungal

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11673-091	TOLNAFTATE (ANTIFUNGAL LIQUID MAXIMUM STRENGTH) LIQUID [TARGET CORPORATION]	6	Legacy NDC	20240910_b48e1f8f-fb74-366a-e053-2a95a90a22bf.zip

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

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
11673-091-01	11673009101	30 mL in 1 BOTTLE, WITH APPLICATOR (11673-091-01)	30 ml	2021-02-15	0000-00-00	No	No	Current