GNC BIO-REMEDY ARNICA RELIEF

Manufacturer
Homeocare Laboratories
Effective date
2018-12-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:30:23

Label at a glance#

ProductGNC BIO-REMEDY ARNICA RELIEF
Active ingredientARNICA MONTANA
Label structure8 sections

Dosage and administration

Chew one tablet and allow to dissolve in the mouth. Take one tablet every 30 minutes until symptoms improve, then reduce to every 4 hours or as needed. For adult use only.

Label contents#

Full prescribing information#

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

Arnica Montana 30C (HPUS)

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Lactose, Magnesium Stearate.

Purpose:

OTC - PURPOSE SECTION

Provides homeopathic relief for pain, bruising, muscle aches, injuries and pre-and-post surgical support.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Indications & Usage:

INDICATIONS & USAGE SECTION

Temporarily relieves the pain and stiffness of injuries, sprains and muscle aches due to injuries.

Warnings:

WARNINGS SECTION

If you are pregnant or breastfeeding, seek the advice of a healthcare professional before using this product.

pain persists for more than 3 days or if pain, redness or swelling worsens, or new symptoms occur, consult a healthcare professional because these could be signs of a serious condition. Keep this and all medicines put of the reach of children. Do not use if cap seal if broken or missing.

Dosage and Administration:

DOSAGE & ADMINISTRATION SECTION

Chew one tablet and allow to dissolve in the mouth. Take one tablet every 30 minutes until symptoms improve, then reduce to every 4 hours or as needed. For adult use only.

GNC Bio Remedy Arnica Relief Tablets

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of gnc arnica relief tabletsimage of gnc arnica relief tablets

image of gnc arnica relief tablets

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61727-80161727-801-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
LACTOSEJ2B2A4N98GIACT
SUCROSEC151H8M554IACT
ARNICA MONTANAO80TY208ZWACTIB

Source Document#

Source XML · Source PDF

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
d3bf836c-c4cf-3332-e053-2995a90ad95096921cf4-981a-4d76-b0d0-7790e6ef95ca2021-12-22WarningsExact identifier
spl set id: 96921cf4-981a-4d76-b0d0-7790e6ef95ca

Reported adverse events (FAERS/openFDA)#

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