Salicylic acid

Product NDC: 11673-631
Requested package NDC: 11673-631-04
11-digit product format: 116730631
Labeler code: 11673
Product ID: 11673-631_c7b63cd2-58dd-0b31-e053-2a95a90a7ac9
Type: HUMAN OTC DRUG
Nonproprietary name: Medicated Callus Removers Extra Thick
Dosage form: PATCH
Route: TOPICAL
Labeler: Target Corporation
Application: part358F
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2017-12-01
Marketing end: 0000-00-00
Substance: SALICYLIC ACID
Active strength: 40 mg/41
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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	11673-631	11673-631-04	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 · 8 matching rows.

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

Captured / source date, Code, Status table
Captured / source date	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2024-11-09 02:27 UTC · source 2024-11-08	I	Inactivated by FDA	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	I	Inactivated by FDA	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	I	Inactivated by FDA	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	I	Inactivated by FDA	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	I	Inactivated by FDA	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	I	Inactivated by FDA	`1332a3947898…`	`d4bfe170f9cd…`

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
11673-631-04	2024-12-18	C162847	48780-1	f386c64a-248e-0266-e053-dadaa90a7c1a	Target Extra Thick Callus Removers
11673-631-04	2023-01-30	C162847	48780-1	f386c64a-248e-0266-e053-dadaa90a7c1a	Target Extra Thick Callus Removers

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11673-631	SALICYLIC ACID (MEDICATED CALLUS REMOVERS EXTRA THICK) PATCH [TARGET CORPORATION]	5	Legacy NDC	20241220_6e2509ab-ec8f-4e2d-b1b5-0b547a11d319.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
O414PZ4LPZ	SALICYLIC ACID	69-72-7	SALICYLIC ACID

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
11673-631-04	11673063104	4 PATCH in 1 PACKAGE (11673-631-04)	4 patch	2017-12-01	0000-00-00	No	No	Current