meijer

Product NDC: 41250-499
11-digit product format: 412500499
Labeler code: 41250
Product ID: 41250-499_38f991cb-366e-1ce2-e063-6394a90ace1d
Type: HUMAN OTC DRUG
Nonproprietary name: Tolnaftate
Dosage form: CREAM
Route: TOPICAL
Labeler: Meijer Distribution Inc
Application: M005
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2006-02-17
Substance: TOLNAFTATE
Active strength: 10 mg/g
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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 · 12 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
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	41250-499-01	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	41250-499-01	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	41250-499-01	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded product	product		`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	41250-499-01	`8dfbde2a14a4…`	`c9ff85d89658…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded product	product		`e2bbac7714bc…`	`27bdfed8d636…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded package	package	41250-499-01	`e2bbac7714bc…`	`27bdfed8d636…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded product	product		`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	41250-499-01	`9bebd1f3094a…`	`5416666fcb17…`

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: meijer
Brand name suffix: antifungal
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
TOLNAFTATE	10 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
06KB629TKV	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
103951	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
374af35a-b8bb-4784-bfc8-c3342de875ca	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316
d723478e-ad4a-ec23-6bd7-cfe33e1e3840	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
41250-499-01	2023-11-27	C162847	48780-1	9d75b9d0-b440-f424-e053-dadaa90a57ce	meijer ™ antifungal
41250-499-01	2020-01-31	C162847	48780-1	9d75b9d0-b440-f424-e053-dadaa90a57ce	meijer ™ antifungal

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
41250-499-01	meijerantifungal	1 in 1 CARTON	CREAM	1	6
41250-499-01	meijerantifungal	15 g in 1 TUBE	CREAM	15	6
41250-499-02	meijerantifungal	30 g in 1 TUBE	CREAM	30	6
41250-499-02	meijerantifungal	1 in 1 CARTON	CREAM	1	6

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Tolnaftate	ACTIVE INGREDIENT	06KB629TKV	MEIJER ANTIFUNGAL (TOLNAFTATE) CREAM [MEIJER DISTRIBUTION INC]	1
Tolnaftate	ACTIVE MOIETY	06KB629TKV	MEIJER ANTIFUNGAL (TOLNAFTATE) CREAM [MEIJER DISTRIBUTION INC]	1
Butylated Hydroxytoluene	INACTIVE INGREDIENT	1P9D0Z171K	MEIJER ANTIFUNGAL (TOLNAFTATE) CREAM [MEIJER DISTRIBUTION INC]	1
petrolatum	INACTIVE INGREDIENT	4T6H12BN9U	MEIJER ANTIFUNGAL (TOLNAFTATE) CREAM [MEIJER DISTRIBUTION INC]	1
polyethylene glycol 3350	INACTIVE INGREDIENT	G2M7P15E5P	MEIJER ANTIFUNGAL (TOLNAFTATE) CREAM [MEIJER DISTRIBUTION INC]	1
Polyethylene glycol 400	INACTIVE INGREDIENT	B697894SGQ	MEIJER ANTIFUNGAL (TOLNAFTATE) CREAM [MEIJER DISTRIBUTION INC]	1
titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	MEIJER ANTIFUNGAL (TOLNAFTATE) CREAM [MEIJER DISTRIBUTION INC]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
41250-499	MEIJER ANTIFUNGAL (TOLNAFTATE) CREAM [MEIJER DISTRIBUTION INC]	5	Current NDC, Legacy NDC, 4 package rows	20250323_374af35a-b8bb-4784-bfc8-c3342de875ca.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 28 of 49 · 973 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Cura Hongo Antifungal	CLOTRIMAZOLE	Pharmadel LLC	df031309-2778-00cf-e053-2a95a90a5eea	2025-11-17	Warnings	Exact identifier application number: M005
CharmTex All in One Antibacterial Shave Gel Body Wash	BENZETHONIUM CHLORIDE	Liufangjing Biotechnology (Yangzhou) Co., Ltd	a7433f39-a8d9-4c78-864d-d7ef193a7daf	2025-11-16	Warnings	Exact identifier application number: M005
Mint Blast Foot and Shoe Antifungal	UNDECYLENIC ACID 10%	SANSAR, LLC	f7fcac19-7b72-4b7a-a28e-669a0eebec9c	2025-11-15	Warnings	Exact identifier application number: M005
Lavender Foot and Shoe Antifungal	UNDECYLENIC ACID 10%	SANSAR, LLC	9db58924-a84d-4763-badb-b3aeb46e1ea6	2025-11-15	Warnings	Exact identifier application number: M005
Citrus Detox Foot and Shoe Antifungal	UNDECYLENIC ACID 10%	SANSAR, LLC	6585c9f5-a6cb-4534-9a61-ecbb6dcb7bdc	2025-11-15	Warnings	Exact identifier application number: M005
AlphaTip Nail Repair Pen	NAIL REPAIR PEN	Guangzhou Qiexiran Cosmetics Co., Ltd.	435c7973-8a67-8f51-e063-6394a90af58f	2025-11-11	Warnings	Exact identifier application number: M005
Pharmlitalia Antifungal Medicated Body	TOLNAFTATE	Foshan Sugar Max Cosmetics CO.,Ltd	399302d2-0da4-4167-8884-b34a9aba8686	2025-11-10	Warnings	Exact identifier application number: M005
PerfectHeal Antifungal	CLOTRIMAZOLE	Zhejiang Dingtai Pharmaceutical Co., Ltd	d9750991-8f10-4d6b-8841-bea022d5ad73	2025-11-10	Warnings	Exact identifier application number: M005
PiYanPing Antifungal	MICONAZOLE NITRATE	Zhejiang Dingtai Pharmaceutical Co., Ltd	840364aa-d799-4163-a9e8-3f10c18f86ae	2025-11-10	Warnings	Exact identifier application number: M005
SKINHEAL ANTIFUNGAL	TOLNAFTATE	Zhejiang Dingtai Pharmaceutical Co., Ltd	570ee9fb-a495-4a99-9215-0cd1bb2e0290	2025-11-10	Warnings	Exact identifier application number: M005
HUA TUO XIAN GAO ANTIFUNGAL	CLOTRIMAZOLE	MADISON ONE ACME INC	e11c4d87-8dc2-44b1-bf6b-12e7ef4f3d1d	2025-11-10	Warnings	Exact identifier application number: M005
Selan Antifungal	SELAN ANTIFUNGAL	Trividia Manufacturing Solutions, Inc	8c7e51a0-0cd5-4ae3-a904-fad7ac6c1a29	2025-11-07	Warnings	Exact identifier application number: M005
Fortinia Ultra	CLOTRIMAZOLE 1%	The Podiatree Company	43065a59-fb81-b1c2-e063-6294a90a36e0	2025-11-07	Warnings	Exact identifier application number: M005
MICOCLEAR	CLOTRIMAZOLE ANTIFUNGAL	Rising Pharma Holdings, Inc.	d75b7d3c-3f1c-47e1-8122-4645f56a444e	2025-11-06	Warnings	Exact identifier application number: M005
Medline	MICONAZOLE NITRATE	Medline Industries, LP	1ea444eb-f2f5-8c63-e063-6294a90acac8	2025-11-06	Warnings	Exact identifier application number: M005
Miconazole Nitrate	ANTIFUNGAL POWDER SPRAY	Premier Brands of America Inc.	38ccf19c-2290-ad99-e063-6394a90a5469	2025-11-06	Warnings	Exact identifier application number: M005
Tolnaftate	ANTIFUNGAL POWDER SPRAY WITH BAKING SODA	Target Corporation	37792b12-c3dc-558f-e063-6294a90a7e75	2025-11-06	Warnings	Exact identifier application number: M005
Tolnafate	TOLNAFTATE POWDER SPRAY	Topco Associates LLC	5f8ae9ab-5e34-7a60-e053-2991aa0a9817	2025-11-06	Warnings	Exact identifier application number: M005
Tolnaftate	TOLNAFTATE JOCK ITCH POWDER SPRAY TALC FREE	Topco Associates LLC	5f8ac6b7-c46c-226c-e053-2991aa0a9606	2025-11-06	Warnings	Exact identifier application number: M005
Tolnaftate	ANTIFUNGAL LIQUID SPRAY	Topco Associates LLC	3dd0df06-3c74-4c34-a69e-4240945f5fa5	2025-11-06	Warnings	Exact identifier application number: M005

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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
103951	tolnaftate 1 % Topical Cream	PSN	374af35a-b8bb-4784-bfc8-c3342de875ca	6
103951	tolnaftate 10 MG/ML Topical Cream	SCD	374af35a-b8bb-4784-bfc8-c3342de875ca	6
103951	tolnaftate 1 % Topical Cream	SY	374af35a-b8bb-4784-bfc8-c3342de875ca	6

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
41250-499-01	41250049901	1 TUBE in 1 CARTON (41250-499-01) / 15 g in 1 TUBE	1 tube	2006-02-17	No	No	Current
41250-499-02	41250049902	1 TUBE in 1 CARTON (41250-499-02) / 30 g in 1 TUBE	1 tube	2006-02-17	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
meijer ™ antifungal	Meijer Distribution Inc \| Sun Pharma Canada Inc.	2025-07-02	HUMAN OTC DRUG LABEL	6