Oxalis 5X

Manufacturer: Uriel Pharmacy, Inc
Effective date: 2026-02-02
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:36:56

Label at a glance#

ProductOxalis 5X

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 Ingredient: Oxalis (Wood sorrel) 5X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Sunflower seed oil, Lanolin, Water, Beeswax, Lanolin alcohol

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Use: 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
Made with care by Uriel, East Troy, WI 53120
shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Oxalis 5X Ointment

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-7224-5	Oxalis 5X	60 g in 1 TUBE	OINTMENT	60		1

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Oxalis 5X
OXALIS STRICTA WHOLE
LANOLIN ALCOHOL
WATER
LANOLIN
BEESWAX
SUNFLOWER OIL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-7224	48951-7224-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
OXALIS STRICTA WHOLE	3STW243384	ACTIB
LANOLIN ALCOHOL	884C3FA9HE	IACT
WATER	059QF0KO0R	IACT
LANOLIN	7EV65EAW6H	IACT
BEESWAX	2ZA36H0S2V	IACT
SUNFLOWER OIL	3W1JG795YI	IACT

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 5X	OXALIS 5X	Uriel Pharmacy, Inc	49de8ed6-b5e8-e8ea-e063-6394a90ad071	2026-02-02	Warnings	Exact identifier ndc (package): 48951-7224-5 ndc (product): 48951-7224 ndc11 (package): 48951722405 spl id: 49de8ed6-b5e9-e8ea-e063-6394a90ad071 spl set id: 49de8ed6-b5e8-e8ea-e063-6394a90ad071

Reported adverse events (FAERS/openFDA)#

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