FDA.reportPublic FDA data

Oxalis 3 Special Order

Product NDC
48951-7174
11-digit product format
489517174
Labeler code
48951
Product ID
48951-7174_6dea3e61-f0a6-f755-e053-2991aa0a32a9
Type
HUMAN OTC DRUG
Nonproprietary name
Oxalis 3 Special Order
Dosage form
PELLET
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
OXALIS STRICTA WHOLE
Active strength
3 [hp_X]/1
NDC exclude flag
No
Listing certified through
2020-12-31
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 productproduct48951-7174IInactivated by FDA2026-08-03
excluded packagepackage48951-717448951-7174-2IInactivated by FDA2026-08-03

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-7174-2Oxalis 3 Special Order1350 in 1 BOTTLE, GLASSPELLET13501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-7174OXALIS 3 SPECIAL ORDER PELLET [URIEL PHARMACY INC.]1Legacy NDC, 1 package rows20180605_6dea3e61-f0a5-f755-e053-2991aa0a32a9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-7174-2489517174021350 PELLET in 1 BOTTLE, GLASS (48951-7174-2) 1350 pellet2009-09-010000-00-00NoNoCurrent