Home NDC 71447-122-01 DR HOS PAIN RELIEF MAXIMUM STRENGTH
Product NDC 71447-122
Requested package NDC 71447-122-01
11-digit product format 714470122
Labeler code 71447
Product ID 71447-122_d7c12015-dca1-4ab1-e053-2a95a90a480c
Type HUMAN OTC DRUG
Nonproprietary name Camphor,Menthol
Dosage form AEROSOL, SPRAY
Route TOPICAL
Labeler LABORATOIRES DRUIDE INC
Application part348
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2022-02-01
Marketing end 0000-00-00
Substance MENTHOL
Active strength 3 g/100mL
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 · 7 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 2025-01-11 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# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71447-122-01 71447012201 1 BOX in 1 BOTTLE, SPRAY (71447-122-01) > 118 mL in 1 BOX (71447-122-00) 1 box 2022-02-01 0000-00-00 No No Current