What is NDC 10893-540?

10893-540 is the product NDC for Naturasil Warts (thuja occidentalis), Thuja occidentalis leafy twig 6 [hp_X]/mL liquid, listed with the FDA by Nature's Innovation, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Naturasil Warts (Thuja Occidentalis).

Nature's Innovation, Inc., NDC labeler code 10893. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Naturasil Warts?

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.

Naturasil Warts NDC 10893-540 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)10893-540Labeler and product segments. Claims need a package NDC.

Product NDC at billing width10893-0540Add 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
10893-540-15	10893054015	15 mL in 1 BOTTLE, GLASS (10893-540-15)Marketed from Oct 1, 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): Naturasil WartsSuffix: Warts
Generic name (nonproprietary): thuja occidentalis
Active ingredients: Thuja occidentalis leafy twig — 6 [hp_X]/mL
Dosage form: Liquid
Route: Topical
Labeler: Nature's Innovation, Inc.NDC labeler code 10893
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 1, 2011
Listing expires: Dec 31, 2026
Identifiers: Product ID 10893-540_70ebc7f1-7879-42e5-82c4-dbd053079ab9SPL ID 70ebc7f1-7879-42e5-82c4-dbd053079ab9SPL set ID a8396d10-ff5b-4f5d-a320-a46c6d788df5UNII 1NT28V9397UPC 0855822001694

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

N410893054015 followed by a unit qualifier and the quantity

Package 10893-0540-15. 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 Jul 25, 2025.

Indications (excerpt from the label)

Uses Uses: Symptomatic treatment of common warts, verruca vulgaris, plantar's warts and flat warts.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 10893-540

What is NDC 10893-540?: 10893-540 is the product NDC for Naturasil Warts (thuja occidentalis), Thuja occidentalis leafy twig 6 [hp_X]/mL liquid, listed with the FDA by Nature's Innovation, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Naturasil Warts (Thuja Occidentalis).
What is the active ingredient?: Thuja occidentalis leafy twig.
Who is the labeler?: Nature's Innovation, Inc., NDC labeler code 10893. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Naturasil Warts?: 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.

Naturasil Warts (Thuja occidentalis) NDC 10893-540