NDC codes

FDA NDC Directory
Product NDC (as listed)51885-9489Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51885-9489Add 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 NDC11-digit (billing)PackageCopy
51885-9489-8518859489081 TUBE in 1 CARTON (51885-9489-8) / 100 g in 1 TUBEMarketed from Sep 22, 2021

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)
Zeel
Generic name (nonproprietary)
alpha lipoic acid, arnica montana whole,sus scrofa cartilage, coenzyme a,solanum dulcamara top,sus scrofa embryo,sus scrofa umbilical cord, nadide, sodium diethyl oxalacetate,sus scrofa placenta,toxicodendron pubescens leaf, sanguinaria canadensis root, silicon dioxide,sulfur,coriander
Active ingredients
Alpha lipoic acid — 6 [hp_X]/gArnica montana whole — 2 [hp_X]/gSus scrofa cartilage — 2 [hp_X]/gCoenzyme a — 6 [hp_X]/gSolanum dulcamara top — 2 [hp_X]/gSus scrofa embryo — 2 [hp_X]/gSus scrofa umbilical cord — 2 [hp_X]/gNadide — 6 [hp_X]/gSodium diethyl oxalacetate — 6 [hp_X]/gSus scrofa placenta — 2 [hp_X]/gToxicodendron pubescens leaf — 2 [hp_X]/gSanguinaria canadensis root — 2 [hp_X]/gSilicon dioxide — 6 [hp_X]/gSulfur — 6 [hp_X]/gCoriander — 8 [hp_X]/g
Dosage form
Ointment
Route
Topical
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 51885-9489_49ef1c5d-a07b-4bc0-9de1-dc40d8477d8fSPL ID 49ef1c5d-a07b-4bc0-9de1-dc40d8477d8fSPL set ID d5d7a2e5-a6ce-4a41-9430-1378023aa7d0UNII 73Y7P0K73Y, O80TY208ZW, 73ECW5WG2F, SAA04E81UX, KPS1B1162N, 9928MC12VO, 118OYG6W3H, 0U46U6E8UK, 6CA025Y4FG, C8CV8867O8, 6IO182RP7A, N9288CD508, ETJ7Z6XBU4, 70FD1KFU70, 1OV56052IK

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

N451885948908 followed by a unit qualifier and the quantity

Package 51885-9489-08. 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 .

Indications (excerpt from the label)

Indications Indications: For the temporary relief of minor arthritis pain and joint stuffness.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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