Search by Drug Name or NDC

NDC 71742-0002-01 Arthri-Joint 30; 30; 30; 30; 30; 30; 30; 30; 30; 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL Details

Arthri-Joint 30; 30; 30; 30; 30; 30; 30; 30; 30; 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL

Arthri-Joint is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Guangzhou Renuma Medical Systems Co., Ltd. The primary component is APIS MELLIFERA; BRYONIA ALBA ROOT; CAUSTICUM; COLCHICUM AUTUMNALE BULB; KALMIA LATIFOLIA LEAF; LEDUM PALUSTRE TWIG; POTASSIUM CARBONATE; PULSATILLA VULGARIS; RHODODENDRON AUREUM LEAF; TOXICODENDRON PUBESCENS LEAF.

Product Information

NDC	71742-0002
Product ID	71742-0002_8344df86-e3cf-425b-b13d-0e1619dced1e
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Arthri-Joint
Proprietary Name Suffix	T008
Non-Proprietary Name	Apis Mellifica, Bryonia (Alba), Causticum, Colchicum Autumnale, Kali Carbonicum, Kalmia Latifolia, Ledum Palustre, Pulsatilla (Vulgaris), Rhododendron Chrysanthum, Rhus Tox
Product Type	HUMAN OTC DRUG
Dosage Form	LIQUID
Route	ORAL
Active Ingredient Strength	30; 30; 30; 30; 30; 30; 30; 30; 30; 30
Active Ingredient Units	[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Substance Name	APIS MELLIFERA; BRYONIA ALBA ROOT; CAUSTICUM; COLCHICUM AUTUMNALE BULB; KALMIA LATIFOLIA LEAF; LEDUM PALUSTRE TWIG; POTASSIUM CARBONATE; PULSATILLA VULGARIS; RHODODENDRON AUREUM LEAF; TOXICODENDRON PUBESCENS LEAF
Labeler Name	Guangzhou Renuma Medical Systems Co., Ltd
Pharmaceutical Class	Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]
DEA Schedule	n/a
Marketing Category	UNAPPROVED HOMEOPATHIC
Application Number	n/a
Listing Certified Through	2024-12-31

Package

Package Images

NDC 71742-0002-01 (71742000201)

Pricing Information	N/A
NDC Package Code	71742-0002-1
Billing NDC	71742000201
Package	59 mL in 1 BOTTLE, DROPPER (71742-0002-1)
Marketing Start Date	2017-10-19
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 3e8e3b3b-498e-4c4a-a096-c06dd8ac3a66 Details

ACTIVE INGREDIENTS:

Apis Mellifica 30X, Bryonia (Alba) 30X, Causticum 30X, Colchicum Autumnale 30X, Kali Carbonicum 30X, Kalmia Latifolia 30X, Ledum Palustre 30X, Pulsatilla (Vulgaris) 30X, Rhododendron Chrysanthum 30X, Rhus Tox 30X.

INDICATIONS:

May temporarily relieve symptoms due to minor joint inflammation and swelling.

WARNINGS:

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

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

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

Store in cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

Adults and children 5 to 10 drops orally, 1 to 2 times daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

May temporarily relieve symptoms due to minor joint inflammation and swelling.

INACTIVE INGREDIENTS:

Demineralized water, Glycerin

QUESTIONS:

Distributed by:

Guangzhou Renuma Medical

Systems Co., Ltd.

No. 5, 2nd Floor, Ascendas 2nd Street

Sino-Singapore Guangzhou Knowledge City

Guangzhou 510555, China

PACKAGE LABEL DISPLAY:

ARTHRI-JOINT

T008

HOMEOPATHIC

2 fl. oz. (59 ml)

INGREDIENTS AND APPEARANCE

ARTHRI-JOINT T008

apis mellifica, bryonia (alba), causticum, colchicum autumnale, kali carbonicum, kalmia latifolia, ledum palustre, pulsatilla (vulgaris), rhododendron chrysanthum, rhus tox liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71742-0002
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z)	APIS MELLIFERA	30 [hp_X] in 1 mL
BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B)	BRYONIA ALBA ROOT	30 [hp_X] in 1 mL
CAUSTICUM (UNII: DD5FO1WKFU) (CAUSTICUM - UNII:DD5FO1WKFU)	CAUSTICUM	30 [hp_X] in 1 mL
COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (COLCHICUM AUTUMNALE BULB - UNII:993QHL78E6)	COLCHICUM AUTUMNALE BULB	30 [hp_X] in 1 mL
POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D)	POTASSIUM CARBONATE	30 [hp_X] in 1 mL
KALMIA LATIFOLIA LEAF (UNII: 79N6542N18) (KALMIA LATIFOLIA LEAF - UNII:79N6542N18)	KALMIA LATIFOLIA LEAF	30 [hp_X] in 1 mL
LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (LEDUM PALUSTRE TWIG - UNII:877L01IZ0P)	LEDUM PALUSTRE TWIG	30 [hp_X] in 1 mL
PULSATILLA VULGARIS (UNII: I76KB35JEV) (ANEMONE PULSATILLA - UNII:I76KB35JEV)	PULSATILLA VULGARIS	30 [hp_X] in 1 mL
RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U) (RHODODENDRON AUREUM LEAF - UNII:IV92NQJ73U)	RHODODENDRON AUREUM LEAF	30 [hp_X] in 1 mL
TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A)	TOXICODENDRON PUBESCENS LEAF	30 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:71742-0002-1	59 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	10/19/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		10/19/2017

Labeler - Guangzhou Renuma Medical Systems Co., Ltd (544538706)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(71742-0002) , api manufacture(71742-0002) , label(71742-0002) , pack(71742-0002)

Revised: 10/2017

Document Id: 8344df86-e3cf-425b-b13d-0e1619dced1e

Set id: 3e8e3b3b-498e-4c4a-a096-c06dd8ac3a66

Version: 2

Effective Time: 20171023

Search by Drug Name or NDC

NDC 71742-0002-01 Arthri-Joint 30; 30; 30; 30; 30; 30; 30; 30; 30; 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL Details

Arthri-Joint 30; 30; 30; 30; 30; 30; 30; 30; 30; 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL

Product Information

Package

Package Images

NDC 71742-0002-01 (71742000201)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL 3e8e3b3b-498e-4c4a-a096-c06dd8ac3a66 Details

ACTIVE INGREDIENTS:

INDICATIONS:

WARNINGS:

KEEP OUT OF REACH OF CHILDREN:

DIRECTIONS:

INDICATIONS:

INACTIVE INGREDIENTS:

QUESTIONS:

PACKAGE LABEL DISPLAY:

INGREDIENTS AND APPEARANCE

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