NDC codes

FDA NDC Directory
Product NDC (as listed)59469-157Labeler and product segments. Claims need a package NDC.
Product NDC at billing width59469-0157Add 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
59469-157-1059469015710594690157101 BOTTLE, GLASS in 1 BOX (59469-157-10) / 50 mL in 1 BOTTLE, GLASSMarketed from May 1, 2005

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)
Thuja
Generic name (nonproprietary)
thuja occidentalis leafy twig
Active ingredients
Thuja occidentalis leafy twig — 3 [hp_X]/50mL
Dosage form
Liquid
Route
Oral
Labeler
PEKANA Naturheilmittel GmbHNDC labeler code 59469
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 59469-157_f076c9c6-31a0-4dff-b7cc-66e08f5ab00eSPL ID f076c9c6-31a0-4dff-b7cc-66e08f5ab00eSPL set ID f5538c6c-9d00-44cb-a097-25d2b027aa9cUNII 1NT28V9397

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

N459469015710 followed by a unit qualifier and the quantity

Package 59469-0157-10. 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 .

Indications (excerpt from the label)

Indications For skin tags and warts. 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 59469-157

What is NDC 59469-157?
59469-157 is the product NDC for Thuja (thuja occidentalis leafy twig), Thuja occidentalis leafy twig 3 [hp_X]/50mL liquid, 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?
Thuja (Thuja occidentalis leafy twig).
What is the active ingredient?
Thuja occidentalis leafy twig.
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 Thuja?
1 other product NDC are listed under this name. See all Thuja 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 Thuja NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
ThujaThuja occidentalis leafy twig 6 [hp_X]/23gGlobuleOralTrue Botanica, LLC53645-122053645-1220-02

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