Home NDC 72668-001-01 Zurflex
Product NDC 72668-001
Requested package NDC 72668-001-01
11-digit product format 726680001
Labeler code 72668
Product ID 72668-001_b3eed442-4346-6cd3-e053-2995a90a59dd
Type HUMAN OTC DRUG
Nonproprietary name Pain Relief Spray
Dosage form SPRAY
Route TOPICAL
Labeler Basler Health Care Group
Application part348
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-07-01
Marketing end 0000-00-00
Substance MENTHOL
Active strength 90 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 · 6 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 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 72668-001-01 72668000101 237 mL in 1 BOTTLE, SPRAY (72668-001-01) 237 ml 2020-07-01 0000-00-00 No No Current