Menthol

Product NDC: 11673-511
11-digit product format: 116730511
Labeler code: 11673
Product ID: 11673-511_c79376de-009e-0e7c-e053-2995a90a3677
Type: HUMAN OTC DRUG
Nonproprietary name: Maximum Strength Medicated Foot Powder Talc Free
Dosage form: POWDER
Route: TOPICAL
Labeler: Target Corporation
Application: part348
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2017-11-27
Marketing end: 0000-00-00
Substance: MENTHOL
Active strength: 3 g/283g
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	11673-511		D	Discontinued by firm		2026-09-09
excluded package	package	11673-511	11673-511-10	D	Discontinued by firm		2026-09-09

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	11673-511-10	`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	11673-511-10	`f5e01cc5f278…`	`a2eaf40c39c3…`

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
11673-511-10	2023-01-31	C162847	48780-1	f386c649-a71e-0266-e053-dadaa90a7c1a	Medicated Foot Powder -Talc Free
11673-511-10	2023-01-30	C162847	48780-1	f386c649-a71e-0266-e053-dadaa90a7c1a	Medicated Foot Powder -Talc Free

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11673-511	MENTHOL (MAXIMUM STRENGTH MEDICATED FOOT POWDER TALC FREE) POWDER [TARGET CORPORATION]	6	Legacy NDC	20241213_cee20e8e-3a44-437b-83ef-0f5303fece2a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
11673-511-10	11673051110	283 g in 1 BOTTLE, PLASTIC (11673-511-10)	283 g	2017-11-27	0000-00-00	No	No	Current