Home NDC 11673-345-60 Pain Relieving
Product NDC 11673-345
Requested package NDC 11673-345-60
11-digit product format 116730345
Labeler code 11673
Product ID 11673-345_efe61d7c-20ae-50e7-e053-2995a90af351
Type HUMAN OTC DRUG
Nonproprietary name Camphor, Menthol, and Methyl Salicylate
Dosage form PATCH
Route TOPICAL
Labeler Target Corporation
Application part348
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2019-03-13
Marketing end 0000-00-00
Substance CAMPHOR (SYNTHETIC); MENTHOL
Active strength 28 mg/1; mg/1
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record
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 · 15 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11673-345-60 Pain Relieving 60 in 1 BOX PATCH 60 3 11673-345-60 Pain Relieving 1 in 1 PATCH PATCH 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11673-345 PAIN RELIEVING (CAMPHOR, MENTHOL, AND METHYL SALICYLATE) PATCH [TARGET CORPORATION] 3 Legacy NDC, 2 package rows 20221217_83ff36dd-9be4-190b-e053-2a91aa0a7ac6.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 11673-345-60 11673034560 60 PATCH in 1 BOX (11673-345-60) > 1 PATCH in 1 PATCH 60 patch 2019-03-13 0000-00-00 No No Current