What is NDC 59469-138?

59469-138 is the product NDC for Zellulisan, Arnica montana root 8 [hp_X]/100g + 7 more ingredients ointment, listed with the FDA by PEKANA Naturheilmittel GmbH. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Zellulisan (Arnica montana root, ledum palustre twig, toxicodendron pubescens shoot, sulfur, horse chestnut, betula pendula leaf, hedera helix flowering twig, and melilotus officinalis top).

What is the active ingredient?

Arnica montana root, Rhododendron tomentosum leafy twig, Toxicodendron pubescens shoot, Sulfur, Horse chestnut, Betula pendula leaf, Hedera helix flowering twig, Melilotus officinalis 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 Zellulisan?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Zellulisan NDC 59469-138 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-138Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0138Add 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
59469-138-30	5946901383059469013830	1 TUBE in 1 BOX (59469-138-30) / 30 g in 1 TUBEMarketed from Dec 11, 2008
59469-138-40	5946901384059469013840	1 TUBE in 1 BOX (59469-138-40) / 100 g in 1 TUBEMarketed from Dec 11, 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): Zellulisan
Generic name (nonproprietary): arnica montana root, ledum palustre twig, toxicodendron pubescens shoot, sulfur, horse chestnut, betula pendula leaf, hedera helix flowering twig, and melilotus officinalis top
Active ingredients: Arnica montana root — 8 [hp_X]/100gRhododendron tomentosum leafy twig — 3 [hp_X]/100gToxicodendron pubescens shoot — 8 [hp_X]/100gSulfur — 15 [hp_X]/100gHorse chestnut — 4 [hp_X]/100gBetula pendula leaf — 8 [hp_X]/100gHedera helix flowering twig — 6 [hp_X]/100gMelilotus officinalis top — 4 [hp_X]/100g
Dosage form: Ointment
Route: Cutaneous
Labeler: PEKANA Naturheilmittel GmbHNDC labeler code 59469
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 11, 2008
Listing expires: Dec 31, 2026
Identifiers: Product ID 59469-138_d5fc8058-6238-444a-a718-1eedb4b81b91SPL ID d5fc8058-6238-444a-a718-1eedb4b81b91SPL set ID 2fe46c61-93d0-45b0-b9bd-356cd7347eb7UNII MUE8Y11327, 877L01IZ0P, 46PYZ1F82M, 70FD1KFU70, 3C18L6RJAZ, 5HW39H9KDH, 3D10KUA6BM, GM6P02J2DX

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N459469013830 followed by a unit qualifier and the quantity

Package 59469-0138-30. 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 20, 2022.

Indications (excerpt from the label)

Uses Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. These "Uses" have not been evaluated by the Food and Drug Administration. With severe forms of this disease, a clinically proven therapy is indicated. For relief of minor tendinitis and inflammation

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59469-138

What is NDC 59469-138?: 59469-138 is the product NDC for Zellulisan, Arnica montana root 8 [hp_X]/100g + 7 more ingredients ointment, listed with the FDA by PEKANA Naturheilmittel GmbH. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Zellulisan (Arnica montana root, ledum palustre twig, toxicodendron pubescens shoot, sulfur, horse chestnut, betula pendula leaf, hedera helix flowering twig, and melilotus officinalis top).
What is the active ingredient?: Arnica montana root, Rhododendron tomentosum leafy twig, Toxicodendron pubescens shoot, Sulfur, Horse chestnut, Betula pendula leaf, Hedera helix flowering twig, Melilotus officinalis 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 Zellulisan?: 1 other product NDC are listed under this name. See all Zellulisan NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Zellulisan NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Zellulisanhorse chestnut, arnica montana, betula pendula leaf, hedera helix flowering twig, ledum palustre twig, melilotus officinalis top, toxicodendron pubescens leaf, and sulfur	Horse chestnut 4 [hp_X]/35g + 7 more ingredients	OintmentTopical	Pekana-Naturheilmittel GmbH	59469-038	59469-0038-35