Oxalis 1X

Manufacturer: Uriel Pharmacy, Inc
Effective date: 2025-01-25
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:31:33

Label at a glance#

ProductOxalis 1X

Active ingredientOXALIS STRICTA WHOLE

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR TOPICAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Apply to skin as needed. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Oxalis extract (Wood sorrel) 1X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Sesame oil, Lanolin, Yellow beeswax, Lanolin alcohol

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Uses: Temporary relief of cramps.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seal is broken or missing.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Oxalis 1X Ointment

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-7214-2	Oxalis 1X	30 g in 1 TUBE	OINTMENT	30		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-7214	OXALIS 1X OINTMENT [URIEL PHARMACY, INC]	1	Current NDC, 1 package rows	20250127_2c907346-28eb-f243-e063-6294a90ae572.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

Oxalis 1X
YELLOW WAX
LANOLIN ALCOHOL
SESAME OIL
LANOLIN
OXALIS STRICTA WHOLE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-7214	48951-7214-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
YELLOW WAX	2ZA36H0S2V	IACT
LANOLIN ALCOHOL	884C3FA9HE	IACT
SESAME OIL	QX10HYY4QV	IACT
LANOLIN	7EV65EAW6H	IACT
OXALIS STRICTA WHOLE	3STW243384	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Oxalis 1X	OXALIS 1X	Uriel Pharmacy, Inc	2c907346-28eb-f243-e063-6294a90ae572	2025-01-25	Warnings	Exact identifier ndc (package): 48951-7214-2 ndc (product): 48951-7214 ndc11 (package): 48951721402 spl id: 2c907346-28ec-f243-e063-6294a90ae572 spl set id: 2c907346-28eb-f243-e063-6294a90ae572

Reported adverse events (FAERS/openFDA)#

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