FDA.reportPublic FDA data

Formica Oxalis

Manufacturer
Uriel Pharmacy, Inc
Effective date
2026-10-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-10-07 01:01:51

Label at a glance#

ProductFormica Oxalis
Active ingredientOXALIS ACETOSELLA LEAF, FORMICA RUFA
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Take 3-4 times daily. Ages 12 and older: 10 drops.
Ages 2-11: 5 drops. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Oxalis e fol. (Wood sorrel) 3X, Formica (Red wood ant) 5X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, 20% Biodynamic organic grape alcohol

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Use: Temporary relief of sore muscles.

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 or if conditions worsen or persist. 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
shopuriel.com Lot: Rev

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Formica Oxalis LiquidFormica Oxalis LiquidFor Oxa Liq

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-420348951-4203-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
OXALIS ACETOSELLA LEAFU1W3U02EW0ACTIB
FORMICA RUFA55H0W83JO5ACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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