Home NDC 72586-004-01 IRxAmigra
Product NDC 72586-004
Requested package NDC 72586-004-01
11-digit product format 725860004
Labeler code 72586
Product ID 72586-004_8577df63-b1dc-4add-b931-2c1eeb4caa7f
Type HUMAN OTC DRUG
Nonproprietary name CAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, and CAPSAICIN
Dosage form LINIMENT
Route TOPICAL
Labeler ActivPower Inc.
Application part348
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-07-01
Marketing end 0000-00-00
Substance CAMPHOR (SYNTHETIC); MENTHOL, UNSPECIFIED FORM; CAPSAICIN
Active strength 100 mg/mL; mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2021-12-31
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 · 18 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…2022-08-30 03:57 UTC · source 2022-08-29 fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 bd6a592717d7…303034d00443…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72586-004-01 IRxAmigra 50 mL in 1 BOTTLE, PLASTIC LINIMENT 50 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72586-004 IRXAMIGRA (CAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, AND CAPSAICIN) LINIMENT [ACTIVPOWER INC.] 1 Legacy NDC, 1 package rows 20200703_216759f6-d5c5-4b53-bf6d-e9bc1881c5f4.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 72586-004-01 72586000401 50 mL in 1 BOTTLE, PLASTIC (72586-004-01) 50 ml 2020-07-01 0000-00-00 No No Current