Oxalis 20%

Manufacturer
Uriel Pharmacy Inc. | Oxalis 20%
Effective date
2024-05-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:26:58

Label at a glance#

ProductOxalis 20%
Active ingredientOXALIS STRICTA WHOLE
Label structure9 sections

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: 20 gm Oxalis (Wood sorrel) 1X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Spring water, Stearic acid, Isopropyl myristate, Lavender oil, Cetyl alcohol, Polyoxyl 40 stearate, Stearyl alcohol, Xanthan gum, Sorbic acid, Tea tree oil, Frankincense oil, Grapefruit seed extract, Myrrh oil

"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: 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. 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, Easy Troy, WI 53120
shopuriel.com Lot#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Oxalis 20 CreamOxalis 20 Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-7198-5Oxalis 20%60 g in 1 TUBECREAM602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-7198OXALIS 20% CREAM [URIEL PHARMACY INC.]2Legacy NDC, 1 package rows20240514_cf32aa91-9c58-1e02-e053-2a95a90ab611.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-719848951-7198-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
185bb8b0-9544-bdf1-e063-6394a90ab232cf32aa91-9c58-1e02-e053-2a95a90ab6112024-05-13WarningsExact identifier
spl id: 185bb8b0-9544-bdf1-e063-6394a90ab232
spl set id: cf32aa91-9c58-1e02-e053-2a95a90ab611

Reported adverse events (FAERS/openFDA)#

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