Berberis Oxalis

Product NDC
48951-2118
11-digit product format
489512118
Labeler code
48951
Product ID
48951-2118_6cb9f706-f1b9-08ed-e053-2991aa0a9934
Type
HUMAN OTC DRUG
Nonproprietary name
Berberis 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
BERBERIS VULGARIS ROOT BARK; OXALIS STRICTA WHOLE; SAW PALMETTO; URTICA URENS; VISCUM ALBUM FRUITING TOP; MAGNESIUM SULFATE, UNSPECIFIED FORM; BOS TAURUS PROSTATE GLAND; PENOXSULAM
Active strength
2 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [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 productproduct48951-2118DDiscontinued by firm2026-10-05
excluded packagepackage48951-211848951-2118-1DDiscontinued 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 packagepackage48951-2118-1d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage48951-2118-1f5e01cc5f278…a2eaf40c39c3…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BERBERIS VULGARIS ROOT BARKACTIVE INGREDIENT1TH8Q20J0UBERBERIS OXALIS LIQUID [URIEL PHARMACY INC.]1
BOS TAURUS PROSTATE GLANDACTIVE INGREDIENT1P66FXU2MWBERBERIS OXALIS LIQUID [URIEL PHARMACY INC.]1
MAGNESIUM SULFATEACTIVE INGREDIENTDE08037SABBERBERIS OXALIS LIQUID [URIEL PHARMACY INC.]1
OXALIS MONTANA LEAFACTIVE INGREDIENTU1W3U02EW0BERBERIS OXALIS LIQUID [URIEL PHARMACY INC.]1
PENOXSULAMACTIVE INGREDIENT784ELC1SCZBERBERIS OXALIS LIQUID [URIEL PHARMACY INC.]1
SAW PALMETTOACTIVE INGREDIENTJ7WWH9M8QSBERBERIS OXALIS LIQUID [URIEL PHARMACY INC.]1
URTICA URENSACTIVE INGREDIENTIHN2NQ5OF9BERBERIS OXALIS LIQUID [URIEL PHARMACY INC.]1
VISCUM ALBUM FRUITING TOPACTIVE INGREDIENTBK9092J5MPBERBERIS OXALIS LIQUID [URIEL PHARMACY INC.]1
BERBERIS VULGARIS ROOT BARKACTIVE MOIETY1TH8Q20J0UBERBERIS OXALIS LIQUID [URIEL PHARMACY INC.]1
BOS TAURUS PROSTATE GLANDACTIVE MOIETY1P66FXU2MWBERBERIS OXALIS LIQUID [URIEL PHARMACY INC.]1
MAGNESIUM CATIONACTIVE MOIETYT6V3LHY838BERBERIS OXALIS LIQUID [URIEL PHARMACY INC.]1
OXALIS MONTANA LEAFACTIVE MOIETYU1W3U02EW0BERBERIS OXALIS LIQUID [URIEL PHARMACY INC.]1
PENOXSULAMACTIVE MOIETY784ELC1SCZBERBERIS OXALIS LIQUID [URIEL PHARMACY INC.]1
SAW PALMETTOACTIVE MOIETYJ7WWH9M8QSBERBERIS OXALIS LIQUID [URIEL PHARMACY INC.]1
URTICA URENSACTIVE MOIETYIHN2NQ5OF9BERBERIS OXALIS LIQUID [URIEL PHARMACY INC.]1
VISCUM ALBUM FRUITING TOPACTIVE MOIETYBK9092J5MPBERBERIS OXALIS LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XBERBERIS OXALIS LIQUID [URIEL PHARMACY INC.]1
waterINACTIVE INGREDIENT059QF0KO0RBERBERIS OXALIS LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-2118BERBERIS OXALIS LIQUID [URIEL PHARMACY INC.]4Legacy NDC20240216_ff96d8ab-3860-443a-8417-c82508e436ff.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-2118-14895121180110 AMPULE in 1 BOX (48951-2118-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent