Reme-D Arnica

Manufacturer
Ilume Technologies, LLC | HomeoCare Laboratories Inc.
Effective date
2017-06-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:15:46

Label at a glance#

ProductReme-D Arnica
Active ingredientARNICA MONTANA FLOWER
Label structure9 sections

Dosage and administration

slightly chew 1-2 tablets and allow to dissolve in the mouth, 3 times a day. For best results avoid eating at least 15 minutes before or after taking the remedy.

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients HPUS: Arnica Montana 30C

Purpose

OTC - PURPOSE SECTION

Pain, bruises, injuries and muscle aches

Warnings

WARNINGS SECTION

Ask a physician before use if pregnant or breast-feeding. Consult a physician if symptoms persist or worsen. Keep out of reach of children. Do not use if inner seal is broken or missing.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Lactose, Magnesium

Stearate

Questions, Comments?

OTC - QUESTIONS SECTION

info@reme-d.com

Call 1-805-324-6966

or visit www.remetush.com

Warnings

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Directions

DOSAGE & ADMINISTRATION SECTION

slightly chew 1-2 tablets and allow to dissolve in the mouth, 3 times a day. For best results avoid eating at least 15 minutes before or after taking the remedy.

Directions

INDICATIONS & USAGE SECTION

slightly chew 1-2 tablets and allow to dissolve in the mouth, 3 times a day. For best results avoid eating at least 15 minutes before or after taking the remedy.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Arnica-FinalArnica-Final

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
71415-00171415-001-60

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
d3bf9720-3e71-d865-e053-2a95a90a47e8516166b4-2b30-140d-e054-00144ff8d46c2021-12-22WarningsExact identifier
spl set id: 516166b4-2b30-140d-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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