Calendula 3X

Manufacturer: Uriel Pharmacy Inc.
Effective date: 2024-09-24
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 02:28:03

Label at a glance#

ProductCalendula 3X

Active ingredientCALENDULA OFFICINALIS FLOWERING TOP

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE.

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: Calendula 3X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Potassium nitrate, Sodium hydroxide, Boric acid, Silver sulfate, Rose oil

Prepared using rhythmical processes

OTC - PURPOSE SECTION

Use: Promotes healing of cuts, grazes and wounds.

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.

REFRIGERATE AFTER OPENING.
USE WITHIN 30 DAYS OF OPENING.
Opened on_________________

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

Calendula 3X 10ml

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-3247-1	Calendula 3X	10 mL in 1 BOTTLE, DROPPER	LIQUID	10		2
48951-3247-1	Calendula 3X	1 in 1 BAG	LIQUID	1		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-3247	CALENDULA 3X LIQUID [URIEL PHARMACY INC.]	2	Legacy NDC, 2 package rows	20240926_c707325f-c2f5-f508-e053-2995a90a9248.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Calendula 3X
BORIC ACID
ROSE OIL
SODIUM HYDROXIDE
SILVER SULFATE
CALENDULA OFFICINALIS FLOWERING TOP
WATER
POTASSIUM NITRATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-3247	48951-3247-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BORIC ACID	R57ZHV85D4	IACT
ROSE OIL	WUB68Y35M7	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
SILVER SULFATE	8QG6HV4ZPO	IACT
CALENDULA OFFICINALIS FLOWERING TOP	18E7415PXQ	ACTIB
WATER	059QF0KO0R	IACT
POTASSIUM NITRATE	RU45X2JN0Z	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
22e32156-75fc-8c16-e063-6394a90a314f			c707325f-c2f5-f508-e053-2995a90a9248	2024-09-24	Warnings	Exact identifier spl id: 22e32156-75fc-8c16-e063-6394a90a314f spl set id: c707325f-c2f5-f508-e053-2995a90a9248

Reported adverse events (FAERS/openFDA)#

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