myDerm Cooling Menthol Pain Relief Roll-On with 50 Percent More Menthol

Product NDC: 72667-022
11-digit product format: 726670022
Labeler code: 72667
Product ID: 72667-022_f1ec39f0-2786-2676-e053-2a95a90a5fde
Type: HUMAN OTC DRUG
Nonproprietary name: Menthol
Dosage form: GEL
Route: TOPICAL
Labeler: Inspec Solutions LLC.
Application: part348
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2021-12-27
Marketing end: 0000-00-00
Substance: MENTHOL
Active strength: 6 g/100mL
NDC exclude flag: No
Listing certified through: 2024-12-31
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	72667-022		D	Discontinued by firm		2026-10-05
excluded package	package	72667-022	72667-022-01	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 · 6 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
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	72667-022-01	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	72667-022-01	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	72667-022-01	`0efc9e666f02…`	`f202fb6c5f17…`

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
72667-022-01	2025-02-01	C162847	48780-1	2cef2736-6f74-d83d-e063-dadaa90ab31f	myDerm Cooling Menthol Pain Relief Roll-On with 50% More Menthol

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72667-022	MYDERM COOLING MENTHOL PAIN RELIEF ROLL-ON WITH 50 PERCENT MORE MENTHOL (MENTHOL) GEL [INSPEC SOLUTIONS LLC.]	11	Legacy NDC	20250202_d4284a1b-dd4f-6bf0-e053-2995a90a6c1e.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
72667-022-01	72667002201	74 mL in 1 BOTTLE, PLASTIC (72667-022-01)	74 ml	2021-12-27	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
myDerm Cooling Menthol Pain Relief Roll-On with 50% More Menthol	Inspec Solutions LLC.	2025-01-31	HUMAN OTC DRUG LABEL	11