Rheuma comp. 102 A

Manufacturer: Uriel Pharmacy. Inc
Effective date: 2024-12-20
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:29:46

Label at a glance#

ProductRheuma comp. 102 A

Active ingredientACONITUM NAPELLUS, MANDRAGORA OFFICINARUM ROOT, ARNICA MONTANA FLOWER, BETULA PUBESCENS LEAF

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

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 Ingredients: Arnica montana 1X, Betula e fol Dec. (Silver birch leaves) 1X, Aconitum napellus (Monkshood) 3X, Mandragora off. (Mandrake) 3X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, 30% Organic cane alcohol

Prepared using rhythmical processes.

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: 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:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Rheuma comp. 102 A Liquid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-8432-3	Rheuma comp. 102 A	60 mL in 1 BOTTLE, DROPPER	LIQUID	60		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-8432	RHEUMA COMP. 102 A LIQUID [URIEL PHARMACY. INC]	1	1 package rows	20241222_29b9eeef-8bd7-e5dd-e063-6394a90a9ae2.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Rheuma comp. 102 A
ACONITUM NAPELLUS
MANDRAGORA OFFICINARUM ROOT
ALCOHOL
ARNICA MONTANA FLOWER
BETULA PUBESCENS LEAF
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-8432	48951-8432-3

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
ACONITUM NAPELLUS	U0NQ8555JD	ACTIB
MANDRAGORA OFFICINARUM ROOT	I2XCB174VB	ACTIB
ALCOHOL	3K9958V90M	IACT
ARNICA MONTANA FLOWER	OZ0E5Y15PZ	ACTIB
BETULA PUBESCENS LEAF	84SOH0O3OO	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
29b9eeef-8bd8-e5dd-e063-6394a90a9ae2			29b9eeef-8bd7-e5dd-e063-6394a90a9ae2	2024-12-20	Warnings	Exact identifier spl id: 29b9eeef-8bd8-e5dd-e063-6394a90a9ae2 spl set id: 29b9eeef-8bd7-e5dd-e063-6394a90a9ae2

Reported adverse events (FAERS/openFDA)#

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