Oxalis 10% Essence

Manufacturer: Uriel Pharmacy Inc.
Effective date: 2018-05-08
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:09:37

Label at a glance#

ProductOxalis 10% Essence

Active ingredientOXALIS STRICTA WHOLE

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

Websitewww.urielpharmacy.com

www.urielpharmacy.com

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR TOPICAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

For compresses: Use 2 teaspoons per cup of lukewarm water. For full bath: Use 2-3 tablespoons.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: 100gm contains: 10gms Oxalis (Wood sorrel) 1X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, 20% Organic cane alcohol

OTC - PURPOSE SECTION

Use: Temporary relief of headache.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings: FOR EXTERNAL USE ONLY.
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. 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
www.urielpharmacy.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Oxalis10Essence

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-7160-6	Oxalis 10% Essence	125 mL in 1 BOTTLE, GLASS	LIQUID	125		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-7160	OXALIS 10% ESSENCE LIQUID [URIEL PHARMACY INC.]	1	Legacy NDC, 1 package rows	20180508_6bb0f068-79a1-face-e053-2a91aa0a7cac.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Oxalis 10% Essence
ALCOHOL
OXALIS STRICTA WHOLE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-7160	48951-7160-6

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	IACT
OXALIS STRICTA WHOLE	3STW243384	ACTIB
WATER	059QF0KO0R	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
6bb0f068-79a2-face-e053-2a91aa0a7cac			6bb0f068-79a1-face-e053-2a91aa0a7cac	2018-05-08	Warnings	Exact identifier spl id: 6bb0f068-79a2-face-e053-2a91aa0a7cac spl set id: 6bb0f068-79a1-face-e053-2a91aa0a7cac

Reported adverse events (FAERS/openFDA)#

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