FDA.reportPublic FDA data

Aralia racemosa

Product NDC
71919-073
11-digit product format
719190073
Labeler code
71919
Product ID
71919-073_7e39c5eb-5731-7043-e053-2991aa0aa060
Type
HUMAN OTC DRUG
Nonproprietary name
ARALIA RACEMOSA ROOT
Dosage form
LIQUID
Route
ORAL
Labeler
Washington Homeopathic Products
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2010-08-09
Marketing end
0000-00-00
Substance
ARALIA RACEMOSA ROOT
Active strength
30 [hp_C]/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 · 5 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct71919-073DDiscontinued by firm2026-08-03
excluded packagepackage71919-07371919-073-07DDiscontinued by firm2026-08-03
excluded packagepackage71919-07371919-073-08DDiscontinued by firm2026-08-03
excluded packagepackage71919-07371919-073-09DDiscontinued by firm2026-08-03
excluded packagepackage71919-07371919-073-10DDiscontinued by firm2026-08-03

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71919-073-077191900730715 mL in 1 VIAL, GLASS (71919-073-07) 15 ml2010-08-090000-00-00NoNoCurrent
71919-073-087191900730830 mL in 1 VIAL, GLASS (71919-073-08) 30 ml2010-08-090000-00-00NoNoCurrent
71919-073-097191900730950 mL in 1 BOTTLE, GLASS (71919-073-09) 50 ml2010-08-090000-00-00NoNoCurrent
71919-073-1071919007310100 mL in 1 BOTTLE, GLASS (71919-073-10) 100 ml2010-08-090000-00-00NoNoCurrent