FDA.reportPublic FDA data

GUNA-ARTHRO

Manufacturer
Guna spa
Effective date
2022-11-15
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 02:18:32

Label at a glance#

ProductGUNA-ARTHRO
Active ingredientSUS SCROFA ARTERY, ASCORBIC ACID, BARIUM OXALOSUCCINATE, BRYONIA ALBA ROOT, CALCITONIN HUMAN, SUS SCROFA CARTILAGE, CHLORINE, BLACK COHOSH, COLCHICUM AUTUMNALE BULB, SUS SCROFA CONJUNCTIVA, SOLANUM DULCAMARA FLOWER, VELAFERMIN, SUS SCROFA UMBILICAL CORD, SUS SCROFA ADRENAL GLAND, NADIDE, SODIUM DIETHYL OXALACETATE, NERVE GROWTH FACTOR, SUS SCROFA PARATHYROID GLAND, SUS SCROFA PLACENTA, QUINHYDRONE, TOXICODENDRON PUBESCENS LEAF, STRONTIUM CARBONATE, SULFUR, SUS SCROFA VEIN, PRASTERONE, .ALPHA.-KETOGLUTARIC ACID, .ALPHA.-LIPOIC ACID
Label structure10 sections

Indications and uses

Temporary relief of minor arthritis symptoms such as: Joint stiffness Joint pain

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 5 drops in a little water 2 times per day

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS/PURPOSE

OTC - ACTIVE INGREDIENT SECTION

ALPHA-KETOGLUTARICUM ACID 3X SUPPORTS CELLULAR RESPIRATION

ALPHA-LIPOIC ACID 3X ANTIOXIDANT

ARTERY 6X PROMOTES METABOLISM

ASCORBIC ACID 3X ANTIOXIDANT

BARIUM OXALOSUCCINATE 3X SUPPORTS CELLULAR RESPIRATION

BRYONIA ALBA 6X, 8X, 12X ANTI-INFLAMMATORY

CALCITONIN 6X PROMOTES MINERALIZATION

CARTILAGO 6X SUPPORTS TISSUE REPAIR

CHLORINUM 6X STRENGTHENS IMMUNE RESPONSE

CIMICIFUGA RACEMOSA 6X, 8X, 12X PAIN RELIEF

COLCHICUM AUTUMNALE 6X, 8X, 12X ANTIOXIDANT

CONJUNCTIVA TISSUE 6X PROMOTES TISSUE REPAIR

DEHYDROEPIANDROSTERONE 6X PROMOTES TISSUE REPAIR

DULCAMARA 6X, 8X, 12X ANTI-INFLAMMATORY

FIBROBLAST GROWTH FACTOR 4C PROMOTES TISSUE REPAIR

FUNICULUS UMBILICALIS 6X SUPPORTS TISSUE REPAIR

GLANDULA SUPRARENALIS 6X ANTI-INFLAMMATORY

NADIDUM 3X PROMOTES CELL METABOLISM

NATRUM OXALACETICUM 3X ANTIOXIDANT

NERVOUS GROWTH FACTOR 4C PAIN RELIEF

PARATHYROID GLAND 6X METABOLIC SUPPORT

PLACENTA TOTALIS 6X REVITALIZING

QUINHYDRONE 3X ANTIOXIDANT

RHUS TOXICODENDRON 6X, 8X, 12X NERVE PAIN RELIEF

STRONTIUM CARBONICUM 6X, 8X, 12X PAIN RELIEF

SULPHUR 3X SENSITIVE SKIN

VEIN 6X PROMOTES METABOLISM


USES

OTC - PURPOSE SECTION

Temporary relief of minor arthritis symptoms such as:

  • Joint stiffness
  • Joint pain

WARNINGS

WARNINGS SECTION

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

PREGNANCY

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding ask a doctor before use

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 5 drops in a little water 2 times per day

QUESTIONS

OTC - QUESTIONS SECTION

Questions?: info@gunainc.com
Tel. (484) 223-3500

INACTIVE INGREDIENT SECTION

Inactive ingredient: Ethyl alcohol 30%.

INDICATIONS & USAGE SECTION

Take 15 minutes before meals

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5USART-ArthroRev06-05-11-185USART-ArthroRev06-05-11-18

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
86ca2ee7-106a-420e-9137-a9ec1af5dbc1Product name120170110
85490a6b-2306-6bf2-c51b-eb63537dc2daProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17089-304-182020-03-13C16284748780-19d75b9d0-48c1-f424-e053-dadaa90a57ceGUNA-ARTHRO
17089-304-182020-01-31C16284748780-19d75b9d0-48c1-f424-e053-dadaa90a57ceGUNA-ARTHRO

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17089-304-18GUNA-ARTHRO30 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS306
17089-304-18GUNA-ARTHRO1 in 1 BOXSOLUTION/ DROPS16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17089-304GUNA-ARTHRO (.ALPHA.-KETOGLUTARIC ACID - ALPHA LIPOIC ACID - ASCORBIC ACID - BARIUM OXALOSUCCINATE - BLACK COHOSH - BRYONIA ALBA ROOT - CALCITONIN HUMAN - CHLORINE - COLCHICUM AUTUMNALE BULB - NADIDE -) SOLUTION/ DROPS [GUNA SPA]6Current NDC, Legacy NDC, 2 package rows20221116_45ad3f03-0ee8-438f-81e7-3ca772022c98.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
.ALPHA.-KETOGLUTARIC ACIDACTIVE INGREDIENT8ID597Z82X2
ALPHA LIPOIC ACIDACTIVE INGREDIENT73Y7P0K73Y2
ASCORBIC ACIDACTIVE INGREDIENTPQ6CK8PD0R2
BARIUM OXALOSUCCINATEACTIVE INGREDIENTL7A49804ZQ2
BLACK COHOSHACTIVE INGREDIENTK73E24S6X92
BRYONIA ALBA ROOTACTIVE INGREDIENTT7J046YI2B2
CALCITONIN HUMANACTIVE INGREDIENTI0IO9290192
CHLORINEACTIVE INGREDIENT4R7X1O28202
COLCHICUM AUTUMNALE BULBACTIVE INGREDIENT993QHL78E62
NADIDEACTIVE INGREDIENT0U46U6E8UK2
NERVE GROWTH FACTORACTIVE INGREDIENTV7FWP1D62O2
PRASTERONEACTIVE INGREDIENT459AG36T1B2
QUINHYDRONEACTIVE INGREDIENTP4A66LQ3QJ2
SODIUM DIETHYL OXALACETATEACTIVE INGREDIENT6CA025Y4FG2
SOLANUM DULCAMARA FLOWERACTIVE INGREDIENTW6J1279A6K2
STRONTIUM CARBONATEACTIVE INGREDIENT41YPU4MMCA2
SULFURACTIVE INGREDIENT70FD1KFU702
SUS SCROFA ADRENAL GLANDACTIVE INGREDIENT398IYQ16YV2
SUS SCROFA ARTERYACTIVE INGREDIENT63O327782Q2
SUS SCROFA CARTILAGEACTIVE INGREDIENT73ECW5WG2F2
SUS SCROFA CONJUNCTIVAACTIVE INGREDIENTW61ME6Q7172
SUS SCROFA PARATHYROID GLANDACTIVE INGREDIENT2KBE35NE8S2
SUS SCROFA PLACENTAACTIVE INGREDIENTC8CV8867O82
SUS SCROFA UMBILICAL CORDACTIVE INGREDIENT118OYG6W3H2
SUS SCROFA VEINACTIVE INGREDIENT2510RH3I892
TOXICODENDRON PUBESCENS LEAFACTIVE INGREDIENT6IO182RP7A2
VELAFERMINACTIVE INGREDIENT6Z25C359272
.ALPHA.-KETOGLUTARIC ACIDACTIVE MOIETY8ID597Z82X2
ALPHA LIPOIC ACIDACTIVE MOIETY73Y7P0K73Y2
ASCORBIC ACIDACTIVE MOIETYPQ6CK8PD0R2
BARIUM OXALOSUCCINATEACTIVE MOIETYL7A49804ZQ2
BLACK COHOSHACTIVE MOIETYK73E24S6X92
BRYONIA ALBA ROOTACTIVE MOIETYT7J046YI2B2
CALCITONIN HUMANACTIVE MOIETYI0IO9290192
CHLORINEACTIVE MOIETY4R7X1O28202
COLCHICUM AUTUMNALE BULBACTIVE MOIETY993QHL78E62
DIETHYL OXALACETATEACTIVE MOIETY15S56468G72
NADIDEACTIVE MOIETY0U46U6E8UK2
NERVE GROWTH FACTORACTIVE MOIETYV7FWP1D62O2
PRASTERONEACTIVE MOIETY459AG36T1B2
QUINHYDRONEACTIVE MOIETYP4A66LQ3QJ2
SOLANUM DULCAMARA FLOWERACTIVE MOIETYW6J1279A6K2
STRONTIUM CATIONACTIVE MOIETY37077S2C932
SULFURACTIVE MOIETY70FD1KFU702
SUS SCROFA ADRENAL GLANDACTIVE MOIETY398IYQ16YV2
SUS SCROFA ARTERYACTIVE MOIETY63O327782Q2
SUS SCROFA CARTILAGEACTIVE MOIETY73ECW5WG2F2
SUS SCROFA CONJUNCTIVAACTIVE MOIETYW61ME6Q7172
SUS SCROFA PARATHYROID GLANDACTIVE MOIETY2KBE35NE8S2
SUS SCROFA PLACENTAACTIVE MOIETYC8CV8867O82
SUS SCROFA UMBILICAL CORDACTIVE MOIETY118OYG6W3H2
SUS SCROFA VEINACTIVE MOIETY2510RH3I892
TOXICODENDRON PUBESCENS LEAFACTIVE MOIETY6IO182RP7A2
VELAFERMINACTIVE MOIETY6Z25C359272
ALCOHOLINACTIVE INGREDIENT3K9958V90M2

Products#

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

DailyMed product names page 1 of 1 · 34 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17089-30417089-304-18

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUS SCROFA ARTERY63O327782QACTIB
ASCORBIC ACIDPQ6CK8PD0RACTIB
BARIUM OXALOSUCCINATEL7A49804ZQACTIB
BRYONIA ALBA ROOTT7J046YI2BACTIB
CALCITONIN HUMANI0IO929019ACTIB
SUS SCROFA CARTILAGE73ECW5WG2FACTIB
CHLORINE4R7X1O2820ACTIB
BLACK COHOSHK73E24S6X9ACTIB
COLCHICUM AUTUMNALE BULB993QHL78E6ACTIB
SUS SCROFA CONJUNCTIVAW61ME6Q717ACTIB
SOLANUM DULCAMARA FLOWERW6J1279A6KACTIB
VELAFERMIN6Z25C35927ACTIB
SUS SCROFA UMBILICAL CORD118OYG6W3HACTIB
SUS SCROFA ADRENAL GLAND398IYQ16YVACTIB
NADIDE0U46U6E8UKACTIB
SODIUM DIETHYL OXALACETATE6CA025Y4FGACTIB
NERVE GROWTH FACTORV7FWP1D62OACTIB
SUS SCROFA PARATHYROID GLAND2KBE35NE8SACTIB
SUS SCROFA PLACENTAC8CV8867O8ACTIB
QUINHYDRONEP4A66LQ3QJACTIB
TOXICODENDRON PUBESCENS LEAF6IO182RP7AACTIB
STRONTIUM CARBONATE41YPU4MMCAACTIB
SULFUR70FD1KFU70ACTIB
SUS SCROFA VEIN2510RH3I89ACTIB
PRASTERONE459AG36T1BACTIB
ALCOHOL3K9958V90MIACT
.ALPHA.-KETOGLUTARIC ACID8ID597Z82XACTIB
.ALPHA.-LIPOIC ACID73Y7P0K73YACTIB

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 22 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MELIXIR / ORAL13675 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MELIXIR / ORAL13675 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSUSPENSION / ORAL681 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / ORAL210 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE / ORAL882 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MTABLET, DELAYED RELEASE / ORALNAExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSUSPENSION / ORAL681 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCONCENTRATE / ORAL198 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / ORAL150.68 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE, EXTENDED RELEASE / ORAL8 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE, EXTENDED RELEASE / ORAL8 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / ORAL210 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / ORAL150.68 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE / ORAL882 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCONCENTRATE / ORAL198 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / ORAL6624 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSYRUP / ORAL21000 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSYRUP / ORAL21000 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MTABLET, DELAYED RELEASE / ORALNAExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / ORAL6624 mgExact identifier — unii+route
22 equally ranked IID candidates

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.ALPHA.-KETOGLUTARIC ACID - ALPHA LIPOIC ACID - ASCORBIC ACID - BARIUM OXALOSUCCINATE - BLACK COHOSH - BRYONIA ALBA ROOT - CALCITONIN HUMAN - CHLORINE - COLCHICUM AUTUMNALE BULB - NADIDE -Guna spa45ad3f03-0ee8-438f-81e7-3ca772022c982022-11-15WarningsExact identifier
ndc (package): 17089-304-18
ndc (product): 17089-304
ndc11 (package): 17089030418
spl id: ed806a9b-af06-d713-e053-2a95a90a9730
spl set id: 45ad3f03-0ee8-438f-81e7-3ca772022c98

Reported adverse events (FAERS/openFDA)#

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