Zellulisan NDC 59469-038

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-038Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0038Add 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
59469-038-35	59469003835	1 TUBE in 1 CARTON (59469-038-35) / 35 g in 1 TUBEMarketed from Feb 20, 2011

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): horse chestnut, arnica montana, betula pendula leaf, hedera helix flowering twig, ledum palustre twig, melilotus officinalis top, toxicodendron pubescens leaf, and sulfur
Active ingredients: Horse chestnut — 4 [hp_X]/35gArnica montana whole — 8 [hp_X]/35gBetula pendula leaf — 8 [hp_X]/35gHedera helix flowering twig — 6 [hp_X]/35gRhododendron tomentosum leafy twig — 3 [hp_X]/35gMelilotus officinalis top — 4 [hp_X]/35gToxicodendron pubescens leaf — 8 [hp_X]/35gSulfur — 15 [hp_X]/35g
Dosage form: Ointment
Route: Topical
Labeler: Pekana-Naturheilmittel GmbH
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 20, 2011
Listing expires: Dec 31, 2026
Identifiers: Product ID 59469-038_a8b74e4c-2f25-42f2-bd53-a9814fe8c3e6SPL ID a8b74e4c-2f25-42f2-bd53-a9814fe8c3e6SPL set ID 50a87245-a81a-4bc6-91b3-257852bfb239UNII 3C18L6RJAZ, O80TY208ZW, 5HW39H9KDH, 3D10KUA6BM, 877L01IZ0P, GM6P02J2DX, 6IO182RP7A, 70FD1KFU70

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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N459469003835 followed by a unit qualifier and the quantity

Package 59469-0038-35. 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 21, 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)