FDA.reportPublic FDA data

ARTHRO PHARMA PAIN RELIEF

Product NDC
71046-001
11-digit product format
710460001
Labeler code
71046
Product ID
71046-001_852b4069-e6f9-3eaa-e053-2a91aa0a69d6
Type
HUMAN OTC DRUG
Nonproprietary name
CAMPHOR (SYNTHETIC)
Dosage form
GEL
Route
TOPICAL
Labeler
Jajy Ventures, LLC
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2016-11-01
Marketing end
0000-00-00
Substance
CAMPHOR (SYNTHETIC)
Active strength
30 mg/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct71046-001DDiscontinued by firm2026-08-03
excluded packagepackage71046-00171046-001-04DDiscontinued by firm2026-08-03

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71046-001-0471046000104118 mL in 1 BOTTLE (71046-001-04) 118 ml2016-11-010000-00-00NoNoCurrent