Berberis Oxalis

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Berberis Oxalis
Generic name: BERBERIS OXALIS
Manufacturer: Uriel Pharmacy Inc.
Product type: HUMAN OTC DRUG
SPL set ID: ff96d8ab-3860-443a-8417-c82508e436ff
SPL ID: 557f0c46-6285-e9a7-e063-6294a90aade5
Version: 6
Effective date: 2026-06-30
Source export date: 2026-10-27
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/b7a5e61d87a3b8f87f4c3ff7b526bfbf6baf84c840f565574c7d83d4083e2b38/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:49:56

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Berberis Oxalis	openfda.brand_name
generic name		BERBERIS OXALIS	openfda.generic_name
manufacturer name		Uriel Pharmacy Inc.	openfda.manufacturer_name
ndc	package	48951-2161-1	openfda.package_ndc
ndc	product	48951-2161	openfda.product_ndc
ndc11	package	48951216101	derived:openfda.package_ndc
spl id		557f0c46-6285-e9a7-e063-6294a90aade5	id
spl set id		ff96d8ab-3860-443a-8417-c82508e436ff	set_id
unii		J7WWH9M8QS	openfda.unii
unii		784ELC1SCZ	openfda.unii
unii		1TH8Q20J0U	openfda.unii
unii		IHN2NQ5OF9	openfda.unii
unii		DE08037SAB	openfda.unii
unii		1P66FXU2MW	openfda.unii
unii		3STW243384	openfda.unii
unii		BK9092J5MP	openfda.unii
unii		KZM8ZRY36A	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings: NOT FOR INJECTION Do not use if allergic to any ingredient. Contains traces of lactose. Consult a physician if symptoms worsen. If pregnant or nursing, consult a physician before use. Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated

Reported adverse events (FAERS/openFDA)#

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