FDA.reportPublic FDA data

GUNA ARTHRO RELIEF

Manufacturer
Guna spa
Effective date
2020-10-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:13:26

Label at a glance#

ProductGUNA ARTHRO RELIEF
Active ingredientOYSTER SHELL CALCIUM CARBONATE, CRUDE, SODIUM SULFATE, .ALPHA.-KETOGLUTARIC ACID, .ALPHA.-LIPOIC ACID, SUS SCROFA ARTERY, ASCORBIC ACID, BARIUM OXALOSUCCINATE, BRYONIA ALBA ROOT, SUS SCROFA CARTILAGE, CHLORINE, BLACK COHOSH, COLCHICUM AUTUMNALE BULB, SUS SCROFA EMBRYO, SOLANUM DULCAMARA FLOWER, SUS SCROFA UMBILICAL CORD, SUS SCROFA ADRENAL GLAND, NADIDE, SODIUM DIETHYL OXALACETATE, SUS SCROFA PLACENTA, TOXICODENDRON PUBESCENS LEAF, SULFUR, SUS SCROFA VEIN
Label structure10 sections

Indications and uses

Temporarily relieves minor arthritic symptoms, such as: Joint stiffness Joint pain Joint swelling and inflammation

Dosage and administration

Adults and children 12 years and older 20 drops in a little water 2 times per day Children between 12 years and 6 years of age 10 drops in a little water 2 times per day Children under 6 years consult a physician

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Take 15 minutes before meals

INACTIVE INGREDIENT SECTION

Inactive ingredient: Ethyl alcohol 30%.

QUESTIONS

OTC - QUESTIONS SECTION

Questions?

info@gunainc.com
(484) 223-3500


WARNINGS

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years and older 20 drops in a little water 2 times per day



Children between 12 years and 6 years of age 10 drops in a little water 2 times per day



Children under 6 years consult a physician

PREGNANCY

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

WARNINGS

WARNINGS SECTION

  • Stop use and ask doctor if symptoms persist more than 5 days.
  • If pregnant or breast-feeding ask a health care professional before use.
  • Keep out of reach of children. In case of overdose, seek professional assistance or contact a Poison Control Center immediately.
  • Contains ethyl alcohol 30%

USES

OTC - PURPOSE SECTION

Temporarily relieves minor arthritic symptoms, such as:

  • Joint stiffness
  • Joint pain
  • Joint swelling and inflammation

ACTIVE INGREDIENTS/PURPOSE

OTC - ACTIVE INGREDIENT SECTION

Arteria suis 6X Helps reduce swelling

Calcarea carbonica 4X Supports bone metabolism

Embryo suis 6X Supports cell metabolism

Funiculus umbilicalis suis 6X Supports bone metabolism

Glandula suprarenalis suis 6X Supports metabolism

Placenta totalis suis 6X Supports metabolism

Ascorbicum acidum 3X Antioxidant

Bryonia alba 6X, 8X, 12X Relieves muscle and joint pain

Cartilago suis 6X Relieves stiffness

Chlorinum 6X Relieves pain

Cimicifuga racemosa 6X, 8X, 12X Relieves rheumatic pain

Colchicum autumnale 6X, 8X, 12X Relieves rheumatic pain

Dulcamara 6X, 8X, 12X Relieves rheumatic pain

Natrum sulphuricum 8X Relieves rheumatic pain

Rhus toxicodendron 6X, 8X, 12X Relieves rheumatic pain

Vena suis 6X Helps reduce swelling

Alpha-ketoglutaricum acidum 3X Supports metabolism

Barium oxalsuccinicum 6X Supports metabolism

Natrum oxalaceticum 3X Supports metabolism

Nadidum 3X Relieves stiffness

Sulphur 4X Relieves stiffness

Alpha-lipoicum acidum 8X Supports metabolism

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5USARR5USARR

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17089-463-18GUNA ARTHRO RELIEF1 in 1 BOXSOLUTION/ DROPS12
17089-463-18GUNA ARTHRO RELIEF30 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17089-463GUNA ARTHRO RELIEF (ARTERIA SUIS - ALPHA KETOGLUTARICUM ACIDUM - ALPHA LIPOICUM ACIDUM - ASCORBICUM ACIDUM - BARIUM OXALSUCCINICUM - BRYONIA ALBA - CALCAREA CARBONICA - CARTILAGO SUIS - CHLORINUM - CIMICIFUGA RACEMOSA - COLCHICUM AUTUMNALE - DULCAMARA - EMBRYO SUIS - FUNICULUS UMBILICALIS SUIS - GLANDULA SUPRARENALIS SUIS - NADIDUM - NATRUM OXALACETICUM - NATRUM SULPHURICUM - PLACENTA TOTALIS SUIS - RHUS TOXICODENDRON - SULPHUR- VENA SUIS -) SOLUTION/ DROPS [GUNA SPA]2Current NDC, Legacy NDC, 2 package rows20201024_aebb990a-65bc-54ed-e053-2995a90a5682.zip

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17089-46317089-463-18

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
OYSTER SHELL CALCIUM CARBONATE, CRUDE2E32821G6IACTIB
SODIUM SULFATE0YPR65R21JACTIB
ALCOHOL3K9958V90MIACT
.ALPHA.-KETOGLUTARIC ACID8ID597Z82XACTIB
.ALPHA.-LIPOIC ACID73Y7P0K73YACTIB
SUS SCROFA ARTERY63O327782QACTIB
ASCORBIC ACIDPQ6CK8PD0RACTIB
BARIUM OXALOSUCCINATEL7A49804ZQACTIB
BRYONIA ALBA ROOTT7J046YI2BACTIB
SUS SCROFA CARTILAGE73ECW5WG2FACTIB
CHLORINE4R7X1O2820ACTIB
BLACK COHOSHK73E24S6X9ACTIB
COLCHICUM AUTUMNALE BULB993QHL78E6ACTIB
SUS SCROFA EMBRYO9928MC12VOACTIB
SOLANUM DULCAMARA FLOWERW6J1279A6KACTIB
SUS SCROFA UMBILICAL CORD118OYG6W3HACTIB
SUS SCROFA ADRENAL GLAND398IYQ16YVACTIB
NADIDE0U46U6E8UKACTIB
SODIUM DIETHYL OXALACETATE6CA025Y4FGACTIB
SUS SCROFA PLACENTAC8CV8867O8ACTIB
TOXICODENDRON PUBESCENS LEAF6IO182RP7AACTIB
SULFUR70FD1KFU70ACTIB
SUS SCROFA VEIN2510RH3I89ACTIB

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
GUNA ARTHRO RELIEFARTERIA SUIS - ALPHA KETOGLUTARICUM ACIDUM - ALPHA LIPOICUM ACIDUM - ASCORBICUM ACIDUM - BARIUM OXALSUCCINICUM - BRYONIA ALBA - CALCAREA CARBONICA - CARTILAGO SUIS - CHLORINUM - CIMICIFUGA RACEMOSA - COLCHICUM AUTUMNALE - DULCAMARA - EMBRYO SUIS - FUNICULUS UMBILICALIS SUIS - GLANDULA SUPRARENALIS SUIS - NADIDUM - NATRUM OXALACETICUM - NATRUM SULPHURICUM - PLACENTA TOTALIS SUIS - RHUS TOXICODENDRON - SULPHUR- VENA SUIS -Guna spaaebb990a-65bc-54ed-e053-2995a90a56822020-10-23WarningsExact identifier
ndc (package): 17089-463-18
ndc (product): 17089-463
ndc11 (package): 17089046318
spl id: b258aa33-c259-1343-e053-2a95a90af0c0
spl set id: aebb990a-65bc-54ed-e053-2995a90a5682

Reported adverse events (FAERS/openFDA)#

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