Oxalis 20%

Manufacturer: Uriel Pharmcy, Inc | Uriel Pharmacy, Inc
Effective date: 2025-08-01
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:34:35

Label at a glance#

ProductOxalis 20%

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: 100 gm contains: 40 gm Oxalis (Wood
sorrel) 1X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Lanolin anhydrous, Sunflower seed oil, Beeswax, Lanolin alcohol, Xanthan gum

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 20 Ointment

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-7221-5	Oxalis 20%	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 20%
LANOLIN ALCOHOL
OXALIS STRICTA WHOLE
YELLOW WAX
LANOLIN
XANTHAN GUM
SUNFLOWER OIL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-7221	48951-7221-5

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
LANOLIN ALCOHOL	884C3FA9HE	IACT
OXALIS STRICTA WHOLE	3STW243384	ACTIB
YELLOW WAX	2ZA36H0S2V	IACT
LANOLIN	7EV65EAW6H	IACT
XANTHAN GUM	TTV12P4NEE	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 20%	OXALIS 20%	Uriel Pharmcy, Inc	3b52ff8d-4b87-d598-e063-6294a90aebd0	2025-08-01	Warnings	Exact identifier ndc (package): 48951-7221-5 ndc (product): 48951-7221 ndc11 (package): 48951722105 spl id: 3b52ff8d-4b88-d598-e063-6294a90aebd0 spl set id: 3b52ff8d-4b87-d598-e063-6294a90aebd0

Reported adverse events (FAERS/openFDA)#

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