What is NDC 59469-143?

59469-143 is the product NDC for Clauparest, Araneus diadematus 9 [hp_X]/50mL + 7 more ingredients solution/ drops, listed with the FDA by PEKANA Naturheilmittel GmbH. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Clauparest (Araneus diadematus, Arnica montana Root, Cupric Acetate, Mandragora officinarum Root, Lead Acetate Anhydrous, Tobacco Leaf, Melilotus officinalis Top, and Ruta graveolens Flowering Top).

What is the active ingredient?

Araneus diadematus, Arnica montana root, Cupric acetate, Mandragora officinarum root, Lead acetate anhydrous, Tobacco leaf, Melilotus officinalis top, Ruta graveolens flowering top.

PEKANA Naturheilmittel GmbH, NDC labeler code 59469. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Clauparest?

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.

Clauparest NDC 59469-143 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-143Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0143Add 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
59469-143-10	5946901431059469014310	1 BOTTLE, GLASS in 1 BOX (59469-143-10) / 50 mL in 1 BOTTLE, GLASSMarketed from Apr 12, 2008

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Clauparest
Generic name (nonproprietary): araneus diadematus, arnica montana root, cupric acetate, mandragora officinarum root, lead acetate anhydrous, tobacco leaf, melilotus officinalis top, and ruta graveolens flowering top
Active ingredients: Araneus diadematus — 9 [hp_X]/50mLArnica montana root — 4 [hp_X]/50mLCupric acetate — 4 [hp_X]/50mLMandragora officinarum root — 6 [hp_X]/50mLLead acetate anhydrous — 6 [hp_X]/50mLTobacco leaf — 6 [hp_X]/50mLMelilotus officinalis top — 4 [hp_X]/50mLRuta graveolens flowering top — 4 [hp_X]/50mL
Dosage form: Solution/ drops
Route: Oral
Labeler: PEKANA Naturheilmittel GmbHNDC labeler code 59469
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 12, 2008
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers: Product ID 59469-143_7aca5451-c6f8-4820-a3a7-a1820546f734SPL ID 7aca5451-c6f8-4820-a3a7-a1820546f734SPL set ID d7ac09b0-b2a8-48d0-8f9f-55478cba2a48UNII 6T6CO7R3Z5, MUE8Y11327, 39M11XPH03, I2XCB174VB, KL498O6790, 6YR2608RSU, GM6P02J2DX, N94C2U587S
Pharmacologic class: Non-Standardized Plant 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

N459469014310 followed by a unit qualifier and the quantity

Package 59469-0143-10. 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 Dec 6, 2022.

Indications (excerpt from the label)

Indications For relief of minor lower body stiffness and pain. Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. With severe forms of this disease, a clinically proven therapy is indicated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59469-143

What is NDC 59469-143?: 59469-143 is the product NDC for Clauparest, Araneus diadematus 9 [hp_X]/50mL + 7 more ingredients solution/ drops, listed with the FDA by PEKANA Naturheilmittel GmbH. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Clauparest (Araneus diadematus, Arnica montana Root, Cupric Acetate, Mandragora officinarum Root, Lead Acetate Anhydrous, Tobacco Leaf, Melilotus officinalis Top, and Ruta graveolens Flowering Top).
What is the active ingredient?: Araneus diadematus, Arnica montana root, Cupric acetate, Mandragora officinarum root, Lead acetate anhydrous, Tobacco leaf, Melilotus officinalis top, Ruta graveolens flowering top.
Who is the labeler?: PEKANA Naturheilmittel GmbH, NDC labeler code 59469. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Clauparest?: 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.