Fibromyalgia Relief® Fast Dissolving Tablets

Manufacturer
TRP Company
Effective date
2025-12-15
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:35:53

Label at a glance#

ProductFibromyalgia Relief
Active ingredientLOESELIA MEXICANA WHOLE, BRYONIA ALBA ROOT, CAUSTICUM, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, PULSATILLA VULGARIS, TOXICODENDRON PUBESCENS LEAF
Label structure12 sections

Indications and uses

• According to homeopathic indications these ingredients provide temporary relief from symptoms such as: • Muscle soreness • Fatigue • Nerve / soft tissue tenderness • Multiple tender points; after serious causes have been ruled out by a physician. * These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Dosage and administration

Suitable for adults and children ages 2 and over. Children under the age of 2: Consult a physician before use. Dissolve entire tablet under tongue. Do not chew or swallow whole. Take 1 tablet 3 times a day or as directed by a physician. Use up to 6 times a day as needed. Take at least 10 minutes before or at least 10 minutes after eating or drinking. • Homeopathic remedies may not be effective for everyone. Indivi...

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Bryonia HPUS 6C, 12C, 18C
Causticum HPUS 6C, 12C, 18C
Hoitzia HPUS 6C, 12C, 18C
Magnesia phosphorica HPUS 6C,12C,18C
Pulsatilla HPUS 6C,12C,18C
Rhus tox HPUS 6C,12C,18C
Valeriana officinalis HPUS 6C,12C,18C

HPUS indicates the active ingredients are in the Homeopathic Pharmacopoeia of the United States.

OTC - PURPOSE SECTION

Bryonia HPUS............................Difficulty moving, Stiff joints, acute soreness
Causticum HPUS.......................Muscle and nerve soreness
Hoitzia HPUS.............................Chronic discomfort, fatigue
Magnesia phosphorica HPUS ...Cramping, Fatigue
Pulsatilla HPUS .........................Migrating soreness
Rhus tox HPUS..........................Soft tissue discomfort
Valeriana officinalis HPUS..........Sleeplessness, Irritable bowels

Uses

INDICATIONS & USAGE SECTION

• According to homeopathic indications these ingredients provide temporary relief from symptoms such as: • Muscle soreness • Fatigue • Nerve / soft tissue tenderness • Multiple tender points; after serious causes have been ruled out by a physician. * These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Suitable for adults and children ages 2 and over. Children under the age of 2: Consult a physician before use.
  • Dissolve entire tablet under tongue.
  • Do not chew or swallow whole.
  • Take 1 tablet 3 times a day or as directed by a physician.
  • Use up to 6 times a day as needed.
  • Take at least 10 minutes before or at least 10 minutes after eating or drinking. • Homeopathic remedies may not be effective for everyone.
  • Individual results may vary. May take up to 60 days to see results.

Other information

SPL UNCLASSIFIED SECTION

• Store at room temperature 15 o to 30 o C (59 o to 86 o F). • Keep bottle tightly closed. • Active ingredients are micro-diluted in accordance with the Homeopathic Pharmacopoeia of the United States and are therefore non-toxic with no known side effects or contraindications. • Fibromyalgia Relief® Fast Dissolving TabletsTM are homeopathic dilutions, for details see www.thereliefproducts.com.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Advantol® 300, Lactose, Magnesium Stearate, Mannitol, Microcrystalline Cellulose.

Do not use if tamper evident seal is torn, broken or missing.

OTC - DO NOT USE SECTION

Do not use if tamper evident seal is torn, broken or missing.

Stop use

OTC - STOP USE SECTION

Stop use and ask a doctor if:

Symptoms persist for more than 7 days or worsen.

Warnings

WARNINGS SECTION

• A PHYSICIAN SHOULD ALWAYS BE CONSULTED TO RULE OUT SERIOUS CAUSES.

• This product is intended to complement, not replace, standard medical treatment.

• Initial worsening of symptoms may occur.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CartonCarton

LabelLabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130858961001716GTIN-13: 0858961001716
EAN-13: 0858961001716
GTIN-12: 858961001716
UPC-A: 858961001716
GTIN storage (14 digits): 00858961001716
TRP_NR_FibroRelief_FDT_70ct_CTN_3-20-24_r7_F.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17312-171-14Fibromyalgia Relief1 in 1 PACKAGETABLET, ORALLY DISINTEGRATING14
17312-171-14Fibromyalgia Relief70 in 1 BOTTLETABLET, ORALLY DISINTEGRATING704

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17312-17117312-171-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Fibromyalgia ReliefBRYONIA ALBA ROOT - CAUSTICUM - LOESELIA MEXICANA WHOLE - MAGNESIUM PHOSPHATE - PULSATILLA VULGARIS - TOXICODENDRON PUBESCENS LEAF - VALERIANTRP Companya6ba3058-ec39-715f-e053-2995a90aa32a2025-12-15WarningsExact identifier
ndc (package): 17312-171-14
ndc (product): 17312-171
ndc11 (package): 17312017114
spl id: 4604abd2-4b86-95d9-e063-6394a90a60d8
spl set id: a6ba3058-ec39-715f-e053-2995a90aa32a

Reported adverse events (FAERS/openFDA)#

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