What is NDC 71742-0002?

71742-0002 is the product NDC for Arthri-Joint T008, Apis mellifera 30 [hp_X]/mL + 9 more ingredients liquid, listed with the FDA by Guangzhou Renuma Medical Systems Co., Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Arthri-Joint T008 (Apis Mellifica, Bryonia (Alba), Causticum, Colchicum Autumnale, Kali Carbonicum, Kalmia Latifolia, Ledum Palustre, Pulsatilla (Vulgaris), Rhododendron Chrysanthum, Rhus Tox).

What is the active ingredient?

Apis mellifera, Bryonia alba root, Causticum, Colchicum autumnale bulb, Potassium carbonate, Kalmia latifolia leaf, Ledum palustre twig, Pulsatilla vulgaris, Rhododendron aureum leaf, Toxicodendron pubescens leaf.

Guangzhou Renuma Medical Systems Co., Ltd, NDC labeler code 71742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Arthri-Joint T008?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Arthri-Joint T008 NDC 71742-0002 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71742-0002Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71742-0002Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
71742-0002-1	7174200020171742000201	59 mL in 1 BOTTLE, DROPPER (71742-0002-1)Marketed from Oct 19, 2017

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Arthri-Joint T008Suffix: T008
Generic name (nonproprietary): apis mellifica, bryonia (alba), causticum, colchicum autumnale, kali carbonicum, kalmia latifolia, ledum palustre, pulsatilla (vulgaris), rhododendron chrysanthum, rhus tox
Active ingredients: Apis mellifera — 30 [hp_X]/mLBryonia alba root — 30 [hp_X]/mLCausticum — 30 [hp_X]/mLColchicum autumnale bulb — 30 [hp_X]/mLPotassium carbonate — 30 [hp_X]/mLKalmia latifolia leaf — 30 [hp_X]/mLLedum palustre twig — 30 [hp_X]/mLPulsatilla vulgaris — 30 [hp_X]/mLRhododendron aureum leaf — 30 [hp_X]/mLToxicodendron pubescens leaf — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Guangzhou Renuma Medical Systems Co., LtdNDC labeler code 71742
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 19, 2017
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 71742-0002_8344df86-e3cf-425b-b13d-0e1619dced1eSPL ID 8344df86-e3cf-425b-b13d-0e1619dced1eSPL set ID 3e8e3b3b-498e-4c4a-a096-c06dd8ac3a66UNII 7S82P3R43Z, T7J046YI2B, DD5FO1WKFU, 993QHL78E6, BQN1B9B9HA, 79N6542N18, 877L01IZ0P, I76KB35JEV, IV92NQJ73U, 6IO182RP7A
Pharmacologic class: Standardized Insect Venom Allergenic Extract

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N471742000201 followed by a unit qualifier and the quantity

Package 71742-0002-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Oct 23, 2017.

Indications (excerpt from the label)

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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71742-0002

What is NDC 71742-0002?: 71742-0002 is the product NDC for Arthri-Joint T008, Apis mellifera 30 [hp_X]/mL + 9 more ingredients liquid, listed with the FDA by Guangzhou Renuma Medical Systems Co., Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Arthri-Joint T008 (Apis Mellifica, Bryonia (Alba), Causticum, Colchicum Autumnale, Kali Carbonicum, Kalmia Latifolia, Ledum Palustre, Pulsatilla (Vulgaris), Rhododendron Chrysanthum, Rhus Tox).
What is the active ingredient?: Apis mellifera, Bryonia alba root, Causticum, Colchicum autumnale bulb, Potassium carbonate, Kalmia latifolia leaf, Ledum palustre twig, Pulsatilla vulgaris, Rhododendron aureum leaf, Toxicodendron pubescens leaf.
Who is the labeler?: Guangzhou Renuma Medical Systems Co., Ltd, NDC labeler code 71742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Arthri-Joint T008?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.