Kapsin

Product NDC
73061-003
11-digit product format
730610003
Labeler code
73061
Product ID
73061-003_aed34082-f268-7f3b-e053-2a95a90ac8c1
Type
HUMAN OTC DRUG
Nonproprietary name
CAMPHOR (SYNTHETIC), CAPSAICIN
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Apipharmausa, LLC
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-09-04
Marketing end
0000-00-00
Substance
CAMPHOR (SYNTHETIC); CAPSAICIN
Active strength
32 mg/g; mg/g
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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct73061-003DDiscontinued by firm2026-10-05
excluded packagepackage73061-00373061-003-60DDiscontinued 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 · 4 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage73061-003-60d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage73061-003-60f5e01cc5f278…a2eaf40c39c3…

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 formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
73061-003-60730610003601 TUBE in 1 BOX (73061-003-60) > 60 g in 1 TUBE1 tube2020-09-040000-00-00NoNoCurrent