Meijer Cold Therapy Roll On

Product NDC: 41250-874
Requested package NDC: 41250-874-21
11-digit product format: 412500874
Labeler code: 41250
Product ID: 41250-874_98561fd4-0bba-05b1-e053-2a95a90a81b7
Type: HUMAN OTC DRUG
Nonproprietary name: MENTHOL
Dosage form: GEL
Route: TOPICAL
Labeler: Meijer Inc.
Application: part348
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2018-10-22
Marketing end: 0000-00-00
Substance: MENTHOL
Active strength: 40 mg/mL
NDC exclude flag: No
Listing certified through: 2020-12-31
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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	41250-874	41250-874-21	D	Discontinued by firm		2026-10-15

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 · 3 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Archive	Snapshot	Source SHA-256
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	41250-874	41250-874-21	I	Inactivated by FDA	excluded / ndc_excluded.zip	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	41250-874	41250-874-21	I	Inactivated by FDA	excluded / ndc_excluded.zip	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	41250-874	41250-874-21	I	Inactivated by FDA	excluded / ndc_excluded.zip	`bd6a592717d7…`	`303034d00443…`

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
41250-874-21	2023-03-07	Meijer Cold Therapy Roll-On
41250-874-25	2023-03-07	Meijer Cold Therapy Roll-On
41250-874-21	2022-01-28	Meijer Cold Therapy Roll-On
41250-874-25	2022-01-28	Meijer Cold Therapy Roll-On

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
41250-874	MEIJER COLD THERAPY ROLL ON (MENTHOL) GEL [MEIJER INC.]	5	Legacy NDC	20230308_3b907ca2-b2c6-4be1-ba4d-d5c2640b0b73.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
41250-874-21	41250087421	74 mL in 1 BOTTLE (41250-874-21)	74 ml	2018-10-22	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Meijer Cold Therapy Roll-On	Meijer Inc. \| Span Packaging Services LLC	2023-03-07	HUMAN OTC DRUG LABEL	5