GUNA 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 ARTHRO RELIEF by

Drug Labeling and Warnings

GUNA ARTHRO RELIEF by is a Homeopathic medication manufactured, distributed, or labeled by Guna spa. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

Take 15 minutes before meals

INACTIVE INGREDIENT

Inactive ingredient: Ethyl alcohol 30%.

QUESTIONS

Questions?

info@gunainc.com
(484) 223-3500

WARNINGS

Keep out of reach of children

DIRECTIONS

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

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

WARNINGS

• 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

Temporarily relieves minor arthritic symptoms, such as:

• Joint stiffness
• Joint pain
• Joint swelling and inflammation

ACTIVE INGREDIENTS/PURPOSE

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

INGREDIENTS AND APPEARANCE

GUNA 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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 17089-463
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I)	OYSTER SHELL CALCIUM CARBONATE, CRUDE	4 [hp_X]  in 30 mL
SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM SULFATE	8 [hp_X]  in 30 mL
.ALPHA.-KETOGLUTARIC ACID (UNII: 8ID597Z82X) (.ALPHA.-KETOGLUTARIC ACID - UNII:8ID597Z82X)	.ALPHA.-KETOGLUTARIC ACID	3 [hp_X]  in 30 mL
.ALPHA.-LIPOIC ACID (UNII: 73Y7P0K73Y) (.ALPHA.-LIPOIC ACID - UNII:73Y7P0K73Y)	.ALPHA.-LIPOIC ACID	8 [hp_X]  in 30 mL
SUS SCROFA ARTERY (UNII: 63O327782Q) (SUS SCROFA ARTERY - UNII:63O327782Q)	SUS SCROFA ARTERY	6 [hp_X]  in 30 mL
ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R)	ASCORBIC ACID	3 [hp_X]  in 30 mL
BARIUM OXALOSUCCINATE (UNII: L7A49804ZQ) (BARIUM CATION - UNII:V645272HLN)	BARIUM OXALOSUCCINATE	6 [hp_X]  in 30 mL
BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B)	BRYONIA ALBA ROOT	6 [hp_X]  in 30 mL
SUS SCROFA CARTILAGE (UNII: 73ECW5WG2F) (SUS SCROFA CARTILAGE - UNII:73ECW5WG2F)	SUS SCROFA CARTILAGE	6 [hp_X]  in 30 mL
CHLORINE (UNII: 4R7X1O2820) (CHLORINE - UNII:4R7X1O2820)	CHLORINE	6 [hp_X]  in 30 mL
BLACK COHOSH (UNII: K73E24S6X9) (BLACK COHOSH - UNII:K73E24S6X9)	BLACK COHOSH	6 [hp_X]  in 30 mL
COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (COLCHICUM AUTUMNALE BULB - UNII:993QHL78E6)	COLCHICUM AUTUMNALE BULB	6 [hp_X]  in 30 mL
SUS SCROFA EMBRYO (UNII: 9928MC12VO) (SUS SCROFA EMBRYO - UNII:9928MC12VO)	SUS SCROFA EMBRYO	6 [hp_X]  in 30 mL
SOLANUM DULCAMARA FLOWER (UNII: W6J1279A6K) (SOLANUM DULCAMARA FLOWER - UNII:W6J1279A6K)	SOLANUM DULCAMARA FLOWER	6 [hp_X]  in 30 mL
SUS SCROFA UMBILICAL CORD (UNII: 118OYG6W3H) (SUS SCROFA UMBILICAL CORD - UNII:118OYG6W3H)	SUS SCROFA UMBILICAL CORD	6 [hp_X]  in 30 mL
SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (SUS SCROFA ADRENAL GLAND - UNII:398IYQ16YV)	SUS SCROFA ADRENAL GLAND	6 [hp_X]  in 30 mL
NADIDE (UNII: 0U46U6E8UK) (NADIDE - UNII:0U46U6E8UK)	NADIDE	3 [hp_X]  in 30 mL
SODIUM DIETHYL OXALACETATE (UNII: 6CA025Y4FG) (DIETHYL OXALACETATE - UNII:15S56468G7)	SODIUM DIETHYL OXALACETATE	3 [hp_X]  in 30 mL
SUS SCROFA PLACENTA (UNII: C8CV8867O8) (SUS SCROFA PLACENTA - UNII:C8CV8867O8)	SUS SCROFA PLACENTA	6 [hp_X]  in 30 mL
TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A)	TOXICODENDRON PUBESCENS LEAF	6 [hp_X]  in 30 mL
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	4 [hp_X]  in 30 mL
SUS SCROFA VEIN (UNII: 2510RH3I89) (SUS SCROFA VEIN - UNII:2510RH3I89)	SUS SCROFA VEIN	6 [hp_X]  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)	9 mL  in 30 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 17089-463-18	1 in 1 BOX	09/24/2020
1		30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		09/24/2020

Labeler - Guna spa (430538264)

Establishment
Name	Address	ID/FEI	Business Operations
Guna spa		338587646	manufacture(17089-463)