FDA.reportPublic FDA data

Carduus Oxalis

Product NDC
48951-3030
11-digit product format
489513030
Labeler code
48951
Product ID
48951-3030_6a9ab41c-d8ea-b95a-e053-2991aa0aae9a
Type
HUMAN OTC DRUG
Nonproprietary name
Carduus Oxalis
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
MILK THISTLE; OXALIS ACETOSELLA LEAF
Active strength
1 [hp_X]/mL; [hp_X]/mL
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 productproduct48951-3030IInactivated by FDA2026-10-05
excluded packagepackage48951-303048951-3030-3IInactivated by FDA2026-10-05

Reported adverse events (FAERS/openFDA)#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-3030-3Carduus Oxalis60 mL in 1 BOTTLE, DROPPERLIQUID603

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MILK THISTLEACTIVE INGREDIENTU946SH95EECARDUUS OXALIS LIQUID [URIEL PHARMACY INC.]1
OXALIS MONTANA LEAFACTIVE INGREDIENTU1W3U02EW0CARDUUS OXALIS LIQUID [URIEL PHARMACY INC.]1
MILK THISTLEACTIVE MOIETYU946SH95EECARDUUS OXALIS LIQUID [URIEL PHARMACY INC.]1
OXALIS MONTANA LEAFACTIVE MOIETYU1W3U02EW0CARDUUS OXALIS LIQUID [URIEL PHARMACY INC.]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MCARDUUS OXALIS LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RCARDUUS OXALIS LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-3030CARDUUS OXALIS LIQUID [URIEL PHARMACY INC.]3Legacy NDC, 1 package rows20180424_211684ac-eb66-4d7c-9c44-b74ec2e45074.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-3030-34895130300360 mL in 1 BOTTLE, DROPPER (48951-3030-3) 60 ml2009-09-010000-00-00NoNoCurrent