Sea Band Motion-Less

Product NDC
0295-8465
Requested package NDC
0295-8465-20
11-digit product format
002958465
Labeler code
0295
Product ID
0295-8465_a110f424-e650-b729-e053-2995a90a9fb8
Type
HUMAN OTC DRUG
Nonproprietary name
Lavandula Angustifolia Oil, Lavandula Hybrida Oil, Mentha Piperita (pepprermint) Oil, Cananga Odorata Flower Oil, Boswellia Carterii Oil, Anthemis Nobilis Flower Oil, Commiphora Myrrha Oil
Dosage form
LIQUID
Route
TOPICAL
Labeler
Denison Pharmaceuticals, LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2020-03-17
Marketing end
0000-00-00
Substance
CHAMAEMELUM NOBILE FLOWER OIL; PEPPERMINT OIL; CANANGA OIL; FRANKINCENSE OIL; LAVENDER OIL; MYRRH OIL; LAVANDIN OIL
Active strength
0 mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage0295-84650295-8465-20DDiscontinued by firm2026-10-05

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 · 12 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0295-8465-20002958465201 TUBE, WITH APPLICATOR in 1 BOTTLE, WITH APPLICATOR (0295-8465-20) > 5 mL in 1 TUBE, WITH APPLICATOR2020-03-170000-00-00NoNoCurrent