Home NDC 71419-001-01 Magic For Pain Relief
Product NDC 71419-001
Requested package NDC 71419-001-01
11-digit product format 714190001
Labeler code 71419
Product ID 71419-001_0ebedb2a-50d0-4204-ad19-2b3c318ba141
Type HUMAN OTC DRUG
Nonproprietary name Camphor, Methyl Salicylate, Menthol
Dosage form SPRAY
Route TOPICAL
Labeler Zhuhai Aofute Medical Technology Co, Ltd
Application part348
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2011-12-01
Marketing end 0000-00-00
Substance CAMPHOR (SYNTHETIC); METHYL SALICYLATE; MENTHOL
Active strength 10 g/100mL; g/100mL; g/100mL
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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71419-001-01 Magic For Pain Relief 30 mL in 1 BOTTLE, PLASTIC SPRAY 30 32707 71419-001-01 Magic For Pain Relief 1 in 1 BOX SPRAY 1 32707
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71419-001 MAGIC FOR PAIN RELIEF (CAMPHOR, METHYL SALICYLATE, MENTHOL) SPRAY [ZHUHAI AOFUTE MEDICAL TECHNOLOGY CO, LTD] 32707 Legacy NDC, 2 package rows 20201209_e468d84e-9469-4d9a-8f95-a2fb9c893e2f.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 71419-001-01 71419000101 1 BOTTLE, PLASTIC in 1 BOX (71419-001-01) > 30 mL in 1 BOTTLE, PLASTIC 2011-12-01 0000-00-00 No No Current