What is NDC 43742-0660?

43742-0660 is the product NDC for Arthritis Joints, Pseudognaphalium obtusifolium 3 [hp_X]/mL + 26 more ingredients liquid, listed with the FDA by Deseret Biologicals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Arthritis Joints (Gnaphalium Polycephalum, Berberis Vulgaris, Cimicifuga Racemosa, Cinchona Officinalis, Colocynthis, Ledum Palustre, Ranunculus Bulbosus, Aesculus Hippocastanum, Borax, Cuprum Aceticum, Kali Carbonicum, Pulsatilla (Vulgaris), Secale Cornutum, Ammonium Muriaticum, Silicea, Argentum Metallicum, Calcarea Phosphorica, Glandula Suprarenalis Suis, Mercurius Praecipitatus Ruber, Sepia, Zincum Metallicum, Palladium Metallicum, Picricum Acidum, Sulphur, Cartilago Suis, Intervertebral Disc (Suis), Medulla Ossis Suis).

What is the active ingredient?

Pseudognaphalium obtusifolium, Berberis vulgaris root bark, Black cohosh, Cinchona officinalis bark, Citrullus colocynthis fruit pulp, Ledum palustre twig, Ranunculus bulbosus, Horse chestnut, Sodium borate, Cupric acetate, Potassium carbonate, Pulsatilla vulgaris, Claviceps purpurea sclerotium, Ammonium chloride, Silicon dioxide, Silver, Tribasic calcium phosphate, Sus scrofa adrenal gland, Mercuric oxide, Sepia officinalis juice, Zinc, Palladium, Picric acid, Sulfur, Sus scrofa cartilage, Sus scrofa intervertebral disc, Sus scrofa bone marrow.

Deseret Biologicals, Inc., NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Arthritis Joints?

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.

Arthritis Joints NDC 43742-0660 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-0660Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-0660Add 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
43742-0660-1	4374206600143742066001	30 mL in 1 BOTTLE, DROPPER (43742-0660-1)Marketed from Nov 11, 2015

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): Arthritis Joints
Generic name (nonproprietary): gnaphalium polycephalum, berberis vulgaris, cimicifuga racemosa, cinchona officinalis, colocynthis, ledum palustre, ranunculus bulbosus, aesculus hippocastanum, borax, cuprum aceticum, kali carbonicum, pulsatilla (vulgaris), secale cornutum, ammonium muriaticum, silicea, argentum metallicum, calcarea phosphorica, glandula suprarenalis suis, mercurius praecipitatus ruber, sepia, zincum metallicum, palladium metallicum, picricum acidum, sulphur, cartilago suis, intervertebral disc (suis), medulla ossis suis
Active ingredients: Pseudognaphalium obtusifolium — 3 [hp_X]/mLBerberis vulgaris root bark — 4 [hp_X]/mLBlack cohosh — 4 [hp_X]/mLCinchona officinalis bark — 4 [hp_X]/mLCitrullus colocynthis fruit pulp — 4 [hp_X]/mLLedum palustre twig — 4 [hp_X]/mLRanunculus bulbosus — 4 [hp_X]/mLHorse chestnut — 6 [hp_X]/mLSodium borate — 6 [hp_X]/mLCupric acetate — 6 [hp_X]/mLPotassium carbonate — 6 [hp_X]/mLPulsatilla vulgaris — 6 [hp_X]/mLClaviceps purpurea sclerotium — 6 [hp_X]/mLAmmonium chloride — 8 [hp_X]/mLSilicon dioxide — 8 [hp_X]/mLSilver — 10 [hp_X]/mLTribasic calcium phosphate — 10 [hp_X]/mLSus scrofa adrenal gland — 10 [hp_X]/mLMercuric oxide — 10 [hp_X]/mLSepia officinalis juice — 10 [hp_X]/mLZinc — 10 [hp_X]/mLPalladium — 12 [hp_X]/mLPicric acid — 12 [hp_X]/mLSulfur — 30 [hp_X]/mLSus scrofa cartilage — 12 [hp_X]/mLSus scrofa intervertebral disc — 12 [hp_X]/mLSus scrofa bone marrow — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.NDC labeler code 43742
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 11, 2015
Marketing end: Oct 16, 2026
Other FDA classes: Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Phosphate Chelating Activity (Mechanism)
Identifiers: Product ID 43742-0660_39ba9cb5-2e09-48f3-b9aa-94d7089297c7SPL ID 39ba9cb5-2e09-48f3-b9aa-94d7089297c7
Pharmacologic class: Blood Coagulation Factor; Phosphate Binder

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

N443742066001 followed by a unit qualifier and the quantity

Package 43742-0660-01. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 43742-0660

What is NDC 43742-0660?: 43742-0660 is the product NDC for Arthritis Joints, Pseudognaphalium obtusifolium 3 [hp_X]/mL + 26 more ingredients liquid, listed with the FDA by Deseret Biologicals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Arthritis Joints (Gnaphalium Polycephalum, Berberis Vulgaris, Cimicifuga Racemosa, Cinchona Officinalis, Colocynthis, Ledum Palustre, Ranunculus Bulbosus, Aesculus Hippocastanum, Borax, Cuprum Aceticum, Kali Carbonicum, Pulsatilla (Vulgaris), Secale Cornutum, Ammonium Muriaticum, Silicea, Argentum Metallicum, Calcarea Phosphorica, Glandula Suprarenalis Suis, Mercurius Praecipitatus Ruber, Sepia, Zincum Metallicum, Palladium Metallicum, Picricum Acidum, Sulphur, Cartilago Suis, Intervertebral Disc (Suis), Medulla Ossis Suis).
What is the active ingredient?: Pseudognaphalium obtusifolium, Berberis vulgaris root bark, Black cohosh, Cinchona officinalis bark, Citrullus colocynthis fruit pulp, Ledum palustre twig, Ranunculus bulbosus, Horse chestnut, Sodium borate, Cupric acetate, Potassium carbonate, Pulsatilla vulgaris, Claviceps purpurea sclerotium, Ammonium chloride, Silicon dioxide, Silver, Tribasic calcium phosphate, Sus scrofa adrenal gland, Mercuric oxide, Sepia officinalis juice, Zinc, Palladium, Picric acid, Sulfur, Sus scrofa cartilage, Sus scrofa intervertebral disc, Sus scrofa bone marrow.
Who is the labeler?: Deseret Biologicals, Inc., NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Arthritis Joints?: 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.